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Cycloheptane, 1,1-dibromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102450-37-3

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102450-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102450-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,5 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102450-37:
(8*1)+(7*0)+(6*2)+(5*4)+(4*5)+(3*0)+(2*3)+(1*7)=73
73 % 10 = 3
So 102450-37-3 is a valid CAS Registry Number.

102450-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dibromocycloheptane

1.2 Other means of identification

Product number -
Other names Cycloheptane,1,1-dibromo

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:102450-37-3 SDS

102450-37-3Upstream product

102450-37-3Relevant academic research and scientific papers

Iodine(III)-Mediated Oxidative Hydrolysis of Haloalkenes: Access to α-Halo Ketones by a Release-and-Catch Mechanism

Jobin-Des Lauriers, Antoine,Legault, Claude Y.

supporting information, p. 108 - 111 (2016/01/15)

An unprecedented iodine(III)-mediated oxidative transposition of vinyl halides has been accomplished. The products obtained, α-halo ketones, are useful and polyvalent synthetic precursors. There are only a handful of reported examples of the direct conversion of vinyl halides to their corresponding α-halo carbonyl compounds. Insights into the mechanism and demonstration that this synthetic transformation can be done under enantioselective conditions are reported.

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