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477952-40-2

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477952-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 477952-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,9,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 477952-40:
(8*4)+(7*7)+(6*7)+(5*9)+(4*5)+(3*2)+(2*4)+(1*0)=202
202 % 10 = 2
So 477952-40-2 is a valid CAS Registry Number.

477952-40-2SDS

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 6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-3-hydroxy-2-methyl-2-nitrohexane

1.2 Other means of identification

Product number -
Other names N-benzyl-N-(tert-butyloxycarbonyl)-4-hydroxy-5-methyl-5-nitrohexylamine

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:477952-40-2 SDS

477952-40-2Relevant articles and documents

Enantioselective alkene radical cations reactions

Crich, David,Shirai, Michio,Brebion, Franck,Rumthao, Sochanchingwung

, p. 6501 - 6518 (2007/10/03)

The reaction of enantiomerically enriched 2-methyl-2-nitro-3-(diphenylphosphatoxy)alkyl radicals with tributyltin hydride and AIBN in benzene at reflux results in the formation of alkene radical cation/anion pairs, which are trapped intramolecularly by am

Enantioselective cyclization of alkene radical cations

Crich, David,Shirai, Michio,Rumthao, Sochanchingwung

, p. 3767 - 3769 (2007/10/03)

(Matrix Presented) Enantiomerically enriched β-(diphenylphosphatoxy) nitroalkanes undergo radical ionic fragmentation, induced by tributyltin hydride and AIBN in benzene at reflux, to give alkene radical cations in contact radical ion pairs. These contact

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