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685902-47-0

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685902-47-0 Usage

General Description

Tert-butyl (5-cyano-2-naphthyl)carbamate is a chemical compound that is used in various research and industrial applications. It is a carbamate derivative that possesses a tert-butyl group and a 5-cyano-2-naphthyl group. TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its unique structure and properties make it a valuable reagent for organic chemistry reactions, including nucleophilic substitution and palladium-catalyzed cross-coupling reactions. Tert-butyl (5-cyano-2-naphthyl)carbamate is known for its stability and compatibility with a wide range of solvents and reagents, making it a versatile chemical building block for the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 685902-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,9,0 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 685902-47:
(8*6)+(7*8)+(6*5)+(5*9)+(4*0)+(3*2)+(2*4)+(1*7)=200
200 % 10 = 0
So 685902-47-0 is a valid CAS Registry Number.

685902-47-0SDS

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 N-(5-cyanonaphthalen-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:685902-47-0 SDS

685902-47-0Relevant articles and documents

Hypoxia-activated prodrugs: Substituent effects on the properties of nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agents

Tercel, Moana,Atwell, Graham J.,Yang, Shangjin,Stevenson, Ralph J.,Botting, K. Jane,Boyd, Maruta,Smith, Eileen,Anderson, Robert F.,Denny, William A.,Wilson, William R.,Pruijn, Frederik B.

scheme or table, p. 7258 - 7272 (2010/07/13)

Nitrochloromethylbenzindolines (nitroCBIs) are a new class of hypoxia-activated prodrugs for antitumor therapy. The recently reported prototypes undergo hypoxia-selective metabolism to form potent DNA minor groove alkylating agents and are selectively tox

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