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Tert-butyl (3-cyanobenzyl)carbamate, with the chemical formula C14H18N2O2, is a carbamate derivative characterized by the presence of a tert-butyl group and a 3-cyanobenzyl group attached to the carbonyl carbon. tert butyl (3 cyanobenzyl)carbaMate is known for its potential applications in various fields, particularly in the pharmaceutical industry, where it serves as an intermediate in the synthesis of drugs. Additionally, it is utilized in research and development for the creation of new molecules with valuable properties. Tert-butyl (3-cyanobenzyl)carbamate may also find uses as an insecticide or in other industrial applications. Given its specific chemical structure and properties, it is crucial to handle tert - butyl (3 - cyanobenzyl)carbaMate with care and adhere to proper safety measures.

916213-93-9

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916213-93-9 Usage

Uses

Used in Pharmaceutical Industry:
Tert-butyl (3-cyanobenzyl)carbamate is used as a chemical intermediate for the synthesis of various drugs, contributing to the development of new pharmaceuticals with potential therapeutic benefits.
Used in Research and Development:
In the realm of research and development, tert-butyl (3-cyanobenzyl)carbamate serves as a building block for the creation of new molecules with potentially valuable properties, expanding the scope of chemical and pharmaceutical innovation.
Used in Insecticide Formulations:
Tert-butyl (3-cyanobenzyl)carbamate may be utilized as an active ingredient or component in insecticide formulations, providing effective pest control solutions in agriculture and other industries.
Used in Other Industrial Applications:
Beyond its pharmaceutical and pesticidal uses, tert-butyl (3-cyanobenzyl)carbamate may also find applications in other industries, capitalizing on its unique chemical properties for specific technical or manufacturing processes.

Check Digit Verification of cas no

The CAS Registry Mumber 916213-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,2,1 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 916213-93:
(8*9)+(7*1)+(6*6)+(5*2)+(4*1)+(3*3)+(2*9)+(1*3)=159
159 % 10 = 9
So 916213-93-9 is a valid CAS Registry Number.

916213-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3-cyanobenzyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 3-cyanobenzylcarbamate

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:916213-93-9 SDS

916213-93-9Relevant academic research and scientific papers

One-pot synthesis of α-amino acids from CO2 using a bismetal reagent with Si-B bond

Mita, Tsuyoshi,Chen, Jianyang,Sugawara, Masumi,Sato, Yoshihiro

, p. 6202 - 6205 (2013/02/23)

In the presence of 1.1 equiv of PhMe2Si-Bpin, 5 equiv of CsF, and 20 mol % of TsOH·H2O, precursors of N-Boc-imines can be converted into the corresponding α-aryl or α-alkenyl glycine derivatives under gaseous CO2 in moderate-to-high yields with a single operation. α-Isobutenyl glycine thus obtained can be further derivatized into various types of α-amino acids including N-Boc-leucine, serine, and glycine derivatives in short steps.

(3-HYDROXY-4-AMINO-BUTAN-2-YL) -3- (2-THIAZOL-2-YL-PYRROLIDINE-1-CARBONYL) BENZAMIDE DERIVATIVES AND RELATED COMPOUNDS AS BETA-SECRETASE INHIBITORS FOR TREATING

-

Page/Page column 117-118, (2009/05/29)

The present invention provides novel beta-secretase inhibitors and methods for their use, including methods of treating of Alzheimer's disease. (Formula)

TRIAZOLE OXADIAZOLES DERIVATIVES

-

Page/Page column 123-124, (2009/07/25)

The invention relates to compounds of formula (I), wherein R1, R2, Ra, Rb, X have the meanings given in claim 1. The compounds are useful e.g. in the treatment of autoimmune disorders, such as multiple sclerosis.

Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 position

Rittle, Kenneth E.,Barrow, James C.,Cutrona, Kellie J.,Glass, Kristen L.,Krueger, Julie A.,Kuo, Lawrence C.,Lewis, S. Dale,Lucas, Bobby J.,McMasters, Daniel R.,Morrissette, Matthew M.,Nantermet, Philippe G.,Newton, Christina L.,Sanders, William M.,Yan, Youwei,Vacca, Joseph P.,Selnick, Harold G.

, p. 3477 - 3482 (2007/10/03)

Thrombin inhibitors incorporating o-aminoalkylbenzylamides in the P1 position were designed, synthesized and found to have enhanced potency and selectivity in several different structural classes. X-ray crystallographic analysis of compound 24 bound in the α-thrombin-hirugen complex provides an explanation for these unanticipated results.

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