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Carbamic acid, (1-cyanopropyl)-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

657424-07-2

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657424-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 657424-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,7,4,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 657424-07:
(8*6)+(7*5)+(6*7)+(5*4)+(4*2)+(3*4)+(2*0)+(1*7)=172
172 % 10 = 2
So 657424-07-2 is a valid CAS Registry Number.

657424-07-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(1-cyanopropyl)carbamate

1.2 Other means of identification

Product number -
Other names 2-BOC-AMINOBUTYRONITRILE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:657424-07-2 SDS

657424-07-2Downstream Products

657424-07-2Relevant academic research and scientific papers

MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS

-

Paragraph 00927, (2017/08/01)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.

Phase transfer catalyzed enantioselective strecker reactions of α-amido sulfones with cyanohydrins

Herrera, Raquel P.,Sgarzani, Valentina,Bernardi, Luca,Fini, Francesco,Pettersen, Daniel,Ricci, Alfredo

, p. 9869 - 9872 (2007/10/03)

A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to effect the enantioselective formation of α-amino nitriles from α-amido sulfones is described. This novel catalytic asymmetric Strecker reaction is analyzed

NEW COMPOUNDS

-

Page/Page column 56, (2010/11/30)

The present invention relates to new compounds of formula (I), wherein P, Q, X1, X2, X3, X4, R, R1, R2, R3, R4, R5, R6, R7, m, n, o, p and q are defined as in any one of claims 1 to 12, a process for their preparation and new intermediates prepared therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.

A convenient synthesis of N-boc-protected α-aminonitriles from α-amidosulfones

Banphavichit, Vorawit,Chaleawlertumpon, Saowaluk,Bhanthumnavin, Worawan,Vilaivan, Tirayut

, p. 3147 - 3160 (2007/10/03)

Synthesis of N-Boc-protected α-aminonitriles starting from N-Boc-protected α-aminosulfones is described. Treatment of the sulfone with two equivalents of potassium cyanide in 2-propanol or dichloromethane- H2O under phase transfer condition affords crystalline N-Boc-protected α-aminonitriles in good yield. Hydrolysis of the aminonitriles provides a convenient access to racemic α-amino acids.

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