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77492-65-0

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77492-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77492-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77492-65:
(7*7)+(6*7)+(5*4)+(4*9)+(3*2)+(2*6)+(1*5)=170
170 % 10 = 0
So 77492-65-0 is a valid CAS Registry Number.

77492-65-0SDS

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 7-(1-adamantyl)-7,8-dihydro-2-methylquinoline

1.2 Other means of identification

Product number -
Other names 7-(1-Adamantyl)-7,8-dihydro-2-methylchinolin

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:77492-65-0 SDS

77492-65-0Downstream Products

77492-65-0Relevant articles and documents

Electrolytic Adamantylation by Reductive Coupling of Quinolinylhalides in the Presence of 1-Bromoadamantane

Hess, U.,Huhn, D.

, p. 381 - 392 (2007/10/02)

Electrochemically generated anion radicals of a number of halogen-substituted quinolines 1a-g dehalogenate in N,N-dimethylformamide to halogen anions and radicals, which may stabilize by hydrogen abstraction from the solvent.In the presence of 1-bromoadamantane the fragments of reductive dehalogenation may be used synthetically for indirect generation of 1-bromoadamantane-radicals, which react predominantly to cross-coupled 2- and 7-monoadamantylated dihydroquinoline- and quinoline-structures, independent of the original halogen position.If C-2 is blocked, adamantylation takes place in the carbocyclic ring.Product distribution and cyclic-voltammetric results are discussed in terms of mechanism.

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