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881426-03-5

Bicyclo[3.1.1]heptan-2-ol, 3-[(1R)-1-(4-methoxyphenyl)ethyl]-6,6-dimethyl-, (1R,2R,3S,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881426-03-5

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881426-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881426-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,4,2 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 881426-03:
(8*8)+(7*8)+(6*1)+(5*4)+(4*2)+(3*6)+(2*0)+(1*3)=175
175 % 10 = 5
So 881426-03-5 is a valid CAS Registry Number.

881426-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R,3S,5S,1'R)-3-(1'-(4-methoxyphenyl)ethyl)-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

1.2 Other means of identification

Product number -
Other names (1R,2R,3S,5S)-3-[(R)-1-(4-Methoxy-phenyl)-ethyl]-6,6-dimethyl-bicyclo[3.1.1]heptan-2-ol

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:881426-03-5 SDS

881426-03-5Downstream Products

881426-03-5Relevant articles and documents

Configuration assignment of stereogenic centers in a β-pinene derivative by 1H NMR and molecular modeling

Perry, Kátia S.P.,Domingos, Jorge L.O.,Dias, Ayres G.,Pinheiro, Sergio,Da Silva, Antonio J.R.,Costa, Paulo R.R.

, p. 157 - 160 (2007/10/03)

The absolute configuration of three contiguous newly generated stereocenters in (1R,2R,3S,5S,1′R)-3-(1′-(4-methoxyphenyl)ethyl)-6, 6-dimethylbicyclo [3.1.1] heptan-2-ol (6), stereoselectively prepared from β-pinene in four steps, was established on the ba

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