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1-methyl-1-nitrocyclohex-3-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

623549-48-4

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623549-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623549-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 623549-48:
(8*6)+(7*2)+(6*3)+(5*5)+(4*4)+(3*9)+(2*4)+(1*8)=164
164 % 10 = 4
So 623549-48-4 is a valid CAS Registry Number.

623549-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-nitrocyclohex-3-ene

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:623549-48-4 SDS

623549-48-4Relevant academic research and scientific papers

Scope of the directed dihydroxylation: Application to cyclic homoallylic alcohols and trihaloacetamides

Donohoe, Timothy J.,Mitchell, Lee,Waring, Michael J.,Helliwell, Madeleine,Bell, Andrew,Newcombe, Nicholas J.

, p. 2173 - 2186 (2003)

The synthesis and directed dihydroxylation of a range of cyclic alkenes was investigated. Both homoallylic alcohols and homoallylic trihaloacetamides were found to be efficient directing groups, giving rise to good to excellent levels of remote asymmetric induction with OsO4-TMEDA. Interestingly, in all cases examined, trifluoroacetamides were found to be superior to trichloroacetamides as directing groups and an argument is presented which rationalises this observation.

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