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3-(BENZYLAMINO)PROPIONITRILE

  • CAS: 706-03-6
  • Purity: 99%
  • Factory Sells Best Quality 3-(BENZYLAMINO)PROPIONITRILE 706-03-6 with GMP standards
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Quality products?make an important contribution to long-term revenue and profitability. Factory Sells Best Quality 3-(BENZYLAMINO)PROPIONITRILE 706-03-6 with GMP standards

1.What is the 3-(BENZYLAMINO)PROPIONITRILE ?

3-(Benzylamino)propionitrile was used as starting reagent in the synthesis of:(3R,4S)-1-benzyl-4-phenylpyrrolidine-3-carboxylic acid, key chiral building block for synthesis of biologically active compounds1-{[benzyl-(2-cyano-ethyl)-amino]-methyl}-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester3-[benzyl-(3,5-dimethyl-pyrazol-1-ylmethyl)-amino]-propionitrile

1-benzylaziridine
1074-42-6

1-benzylaziridine

sodium cyanide
773837-37-9

sodium cyanide

3-(benzylamino)propionitrile
706-03-6

3-(benzylamino)propionitrile

N,N'-dibenzylpiperazine
1034-11-3

N,N'-dibenzylpiperazine

benzaldehyde
100-52-7

benzaldehyde

Conditions
Conditions Yield
With ruthenium(IV) oxide; sodium periodate; water; In chloroform; at 20 ℃;
acrylonitrile
107-13-1,25014-41-9

acrylonitrile

benzylamine
100-46-9

benzylamine

3-(benzylamino)propionitrile
706-03-6

3-(benzylamino)propionitrile

Conditions
Conditions Yield
With copper diacetate; In water; at 20 ℃; for 12h;
98%
iron(III) chloride; In water; at 20 ℃; for 15h;
98%
With poly(ethylene glycol) 2000; ruthenium trichloride; at 50 ℃; for 3h;
96%
With ES-SO3H*Pyridine; In tetrahydrofuran; at 20 ℃; for 0.416667h; solid phase reaction;
95%
With MCM-41 immobilized phenanthrolinium dibromide; In water; at 20 ℃; for 0.5h; Catalytic behavior;
95%
With phosphotungstic acid; In water; at 20 ℃; for 2.5h;
94%
With iodine-alumina; at 20 ℃; for 0.5h; Neat (no solvent);
94%
In water; at 20 ℃; for 0.0833333h; Sonication;
93%
With boric acid; In water; at 20 ℃; for 2.5h;
92%
With samarium(III) trifluoromethanesulfonate; In dichloromethane; at 20 ℃; for 2.5h;
92%
With N,N,N-trimethyl-N-(propanesulfonic acid)ammonium hydrogensulfate; In water; at 20 ℃; for 3h;
92%
With Ps-AlCl3; at 20 ℃; for 2h; chemoselective reaction;
92%
With carbon nanodots; In water; at 25 ℃; for 0.116667h;
92%
With dimethylbromosulphonium bromide; at 20 ℃; for 0.25h;
91%
With vanadyl acetate; at 20 ℃; for 0.833333h;
91%
With iranian dolomite; In water; at 20 ℃; for 1h;
91%
With 2C2H3O2(1-)*Pd(2+)*3Na(1+)*C18H12O9PS3(3-); glycerol; at 100 ℃; for 2h; Schlenk technique; Inert atmosphere;
91%
With lithium perchlorate; at 20 ℃; for 2h;
90%
With 1 mol% HClO4/SiO2; for 0.05h; Neat (no solvent); Microwave irradiation; Inert atmosphere;
90%
With graphene oxide; In water; at 20 ℃; for 0.116667h;
90%
With ZrOCl2*8H2O on montmorillonite K10; at 20 ℃; for 0.25h;
89%
With hydroquinone; Heating;
88%
With TiCl2(OTf ) immobilized on silica gel; In neat (no solvent); at 20 ℃; for 0.166667h;
88%
With cadmium(II) chloride; In dichloromethane; at 20 ℃; for 2.5h;
87%
With borax; In water; at 20 ℃; for 1.5h;
86%
With water; at 20 ℃; for 0.5h;
85%
In methanol; at 20 ℃; for 1.83333h; Reflux;
84%
fipronilβ-cyclodextrin; In water; acetone; at 20 ℃; for 8h;
82%
In water; for 0.05h; Microwave irradiation;
82%
With o-benzenedisulfonimide; In neat (no solvent); at 20 ℃; for 2h;
82%
With aluminum oxide; at 20 ℃; for 4h; Neat (no solvent);
80%
With copper(II) oxide; In methanol; at 20 ℃; for 6h;
77%
With ZSM-5-SO3H zeolite; In neat (no solvent); for 3h; Heating;
75%
With ZSM-5-SO3H; at 50 - 100 ℃; for 3h;
75%
In water; for 75h; Heating;
72%
With iodine; In dichloromethane; at 20 ℃; for 2.5h;
70%
With [(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)Cu(I)(anilido)]; In benzene-d6; at 20 ℃; for 0.0833333h;
100 % Spectr.
In methanol; at 20 ℃; for 3.5h;
polystyrenesulfonic acid; In water; at 80 ℃; under 2068.65 - 3620.13 Torr; microwave irradiation;
85 % Chromat.
With Lipozyme RM IM lipase; In toluene; at 30 ℃; for 1h; Enzymatic reaction;
With tetrachlorosilane; at 0 - 60 ℃; Inert atmosphere; neat (no solvent);
With [(2,6-(iPr2PO)2C6H3-κ3C,P,P')Ni(triflate)]; triethylamine; In toluene; at 50 ℃; for 3h; Inert atmosphere;
With C34H42F6N4O6S2Zr; In benzene-d6; at 20 ℃; for 0.0833333h; Concentration; Reagent/catalyst; Catalytic behavior; Inert atmosphere; Schlenk technique; Glovebox;
97 %Spectr.
With sodium stannate; at 20 ℃; for 4h;
In water; at 15 ℃; for 12h;
32 g

2.What is the CAS number for 3-(BENZYLAMINO)PROPIONITRILE ?

The CAS number of 3-(BENZYLAMINO)PROPIONITRILE is 706-03-6.

More information of 3-(BENZYLAMINO)PROPIONITRILE 706-03-6 are:

CAS?Number

706-03-6

Density

1.017 g/cm3

Melting Point

70 °C

Boiling Point

301.4 °C at 760 mmHg

Flash Point

136.1 °C

Vapor Pressure

0.00106mmHg at 25°C

Refractive Index

n20/D 1.5308(lit.)

HS CODE

29269095

PSA

35.82000

LogP

2.08078

Pka

7.29±0.19(Predicted)

3.What are another words for 3-(BENZYLAMINO)PROPIONITRILE ?

Synonyms?for?3-(BENZYLAMINO)PROPIONITRILE 706-03-6:Propionitrile,3-(benzylamino)- (6CI,7CI,8CI);(2-Cyanoethyl)(phenylmethyl)amine;3-(Benzylamino)propanenitrile;3-(Benzylamino)propionitrile;3-[(Phenylmethyl)amino]propanenitrile;Benzyl(2-cyanoethyl)amine;N-(2-Cyanoethyl)benzylamine;N-(2-Nitrilethyl)benzylamine;N-Benzyl-2-cyanoethylamine;b-(Benzylamino)propionitrile;

4.What is the molecular formula of 3-(BENZYLAMINO)PROPIONITRILE?

The chemical formula of ?3-(BENZYLAMINO)PROPIONITRILE is?C10H12N2 which containing 10 Carbon atoms,12 Hydrogen atoms and 2 Nitrogen atoms,and the molecular weight of??3-(BENZYLAMINO)PROPIONITRILE?is 160.219.

5.What is 3-(BENZYLAMINO)PROPIONITRILE (706-03-6) used for?

3-(Benzylamino)propionitrile is a clear, colorless liquid that is a key intermediate in the synthesis of various biologically active compounds. It is known for its ability to undergo aza-type Michael reactions with 1-hydroxymethyl-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester under mild conditions.

InChI:InChI=1/C10H12N2/c11-7-4-8-12-9-10-5-2-1-3-6-10/h1-3,5-6,12H,4,8-9H2/p+1

Relevant articles related to 3-(BENZYLAMINO)PROPIONITRILE:

Article

Source

TiCl2(OTf)-SiO2: A solid stable lewis acid catalyst for Michael addition of α-Aminophosphonates, Amines, Indoles and Pyrrole

Firouzabadi, Habib,Iranpoor, Naser,Farahi, Soghra

, p. 317 - 323 (2018/02/06)

Synthesis and structure-activity relationship study of arylsulfonamides as novel potent H5N1 inhibitors

Yu, Yongshi,Tang, Qi,Xu, Zhichao,Li, Siliang,Jin, Mengyu,Zhao, Zixuan,Dong, Chune,Wu, Shuwen,Zhou, Hai-Bing

, p. 206 - 216 (2018/10/15)

6.Buy 3-(BENZYLAMINO)PROPIONITRILE with the best price .

Avanscure lifesciences (Shanghai ) Pvt Ltd. is a quality supplier of 3-(BENZYLAMINO)PROPIONITRILE. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on 3-(BENZYLAMINO)PROPIONITRILE 706-03-6.

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