(1S)-1-Cyano-2-methylpropyl acetate

Base Information

Chemical Name:(1S)-1-Cyano-2-methylpropyl acetate
CAS No.:72690-95-0
Molecular Formula:C7H11NO2
Molecular Weight:141.16800
Hs Code.:
DSSTox Substance ID:DTXSID40560456
Nikkaji Number:J434.038H
Wikidata:Q82443848

Synonyms:(1S)-1-Cyano-2-methylpropyl acetate;72690-95-0;DTXSID40560456

Suppliers and Price of (1S)-1-Cyano-2-methylpropyl acetate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of (1S)-1-Cyano-2-methylpropyl acetate

Chemical Property:

PSA：50.09000
LogP:1.09768
XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:141.078978594
Heavy Atom Count:10
Complexity:166

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C#N)OC(=O)C
Isomeric SMILES:CC(C)[C@@H](C#N)OC(=O)C

Technology Process of (1S)-1-Cyano-2-methylpropyl acetate

There total 1 articles about (1S)-1-Cyano-2-methylpropyl acetate 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:

: 151-50-8
potassium cyanide

: 108-24-7
acetic anhydride

: 78-84-2
isobutyraldehyde

: 15344-34-0
2-hydroxy-3-methylbutanenitrile

: 72690-95-0
(S)-O-acetyl-2-hydroxy-3-methylbutanenitrile

: 126567-39-3
(R)-O-acetyl-2-hydroxy-3-methylbutanenitrile

Guidance literature:: potassium cyanide; acetic anhydride; isobutyraldehyde; (S,S)-(salen derivative)titanium; In dichloromethane; water; tert-butyl alcohol; at -40 ℃;

With candida antarctica lipase-B; isopropyl alcohol; In various solvents; at 20 ℃; for 23.5h; Title compound not separated from byproducts;
DOI:10.1002/ejoc.200600467