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77826-32-5

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77826-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77826-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77826-32:
(7*7)+(6*7)+(5*8)+(4*2)+(3*6)+(2*3)+(1*2)=165
165 % 10 = 5
So 77826-32-5 is a valid CAS Registry Number.

77826-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)-cycloheptanol

1.2 Other means of identification

Product number -
Other names 1-(4-Fluoro-phenyl)-cycloheptanol

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:77826-32-5 SDS

77826-32-5Downstream Products

77826-32-5Relevant articles and documents

Iodobenzene-catalyzed oxidative cleavage of olefins to carbonyl compounds

Du, Lele,Wang, Zechao,Wu, Junliang

supporting information, (2020/07/20)

A metal-free approach for the oxidative cleavage of carbon–carbon double bonds of olefins to carbonyl compounds was established by using oxidant m-CPBA and non-metallic organocatalyst PhI in toluene/H2O. A broad scope of aromatic olefins was used. All the reactions proceeded smoothly at 35 °C in short reaction time to furnish the respective mono- and double carbonyl compounds selectively in moderate to good yields.

Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes

Lee, Gon-Ann,Lee, Hsin-Yi,Wang, Wen-Chieh,Cherng, Chih-Hwa

, p. 2956 - 2961 (2014/04/17)

Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes to a new series of [7-6-6] tricyclic system were described. A variety of substituents at the para-position of the phenyl were amenable to this transformation, including electron-donating groups and halides. The presence of electron-donating groups resulted in a more efficient reaction, with higher yields than the case of halides.

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