(2R)-2-methylbutanenitrile

Base Information

Chemical Name:(2R)-2-methylbutanenitrile
CAS No.:137120-33-3
Molecular Formula:C₅H₉N
Molecular Weight:83.1332
Hs Code.:
UNII:R5N74V6P9T
Nikkaji Number:J57.417A

Synonyms:(R)-2-Methylbutanenitrile;(r)-2-methyl-butyronitrile;(2R)-2-methylbutanenitrile;2-Methylbutyronitrile, (R)-;R5N74V6P9T;137120-33-3;Butanenitrile, 2-methyl-, (R)-;Butanenitrile, 2-methyl-, (2R)-;UNII-R5N74V6P9T;[R,(?)]-2-Methylbutyronitrile

Suppliers and Price of (2R)-2-methylbutanenitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (2R)-2-methylbutanenitrile

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:83.073499291
Heavy Atom Count:6
Complexity:67.3

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(C)C#N
Isomeric SMILES:CC[C@@H](C)C#N

Technology Process of (2R)-2-methylbutanenitrile

There total 1 articles about (2R)-2-methylbutanenitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 116-53-0,600-07-7
2-Methylbutanoic acid

: 140-29-4
phenylacetonitrile

: 103-82-2
phenylacetic acid

: 137120-33-3
(R)-2-methyl-butyronitrile

: 25570-03-0
(+)-(S)-2-methylbutane nitrile

Guidance literature:: With sulfuric acid; at 190 ℃; Product distribution; exchange reaction between (+)-(S)-2-methylbutanoic acid (95percent optical purity) and phenylacetonitrile, optical yield, racemization; stereoselective formation of nitrile by the reaction with chlorosulfonylisocyanate under mild conditions;

Reference yield:

: 137120-33-3
(R)-2-methyl-butyronitrile

: Benzyl-((R)-2-methyl-butyl)-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) diisobutylaluminum hydride / 1.) CH₂Cl₂, r.t.; 2.) CH₂Cl₂, 0 deg C

2: NaBH₄ / ethanol / Ambient temperature

With sodium tetrahydroborate; diisobutylaluminium hydride; In ethanol;
DOI:10.1016/S0040-4039(98)00603-0

Reference yield:

: 137120-33-3
(R)-2-methyl-butyronitrile

: 100-46-9
benzylamine

: Benzyl-[(R)-2-methyl-but-(Z)-ylidene]-amine

Guidance literature:: With diisobutylaluminium hydride; Multistep reaction; 1.) CH₂Cl₂, r.t.; 2.) CH₂Cl₂, 0 deg C;
DOI:10.1016/S0040-4039(98)00603-0