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126421-67-8

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126421-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126421-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,2 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126421-67:
(8*1)+(7*2)+(6*6)+(5*4)+(4*2)+(3*1)+(2*6)+(1*7)=108
108 % 10 = 8
So 126421-67-8 is a valid CAS Registry Number.

126421-67-8SDS

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 (R)-(-)-2,2-diphenylcyclopentanol

1.2 Other means of identification

Product number -
Other names (R)-2,2-Diphenylcyclopentanol

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:126421-67-8 SDS

126421-67-8Relevant articles and documents

Enzymatic resolution of hindered secondary alcohols: Efficient access to a new simplified chiral auxiliary

Randrianasolo-Rakotozafy,Azerad,Dumas,Potin,D'Angelo

, p. 761 - 766 (1993)

2,2-Diphenylcyclopentanol, an efficient chiral auxiliary which bears only one stereogenic center, as well as some related hindered secondary alcohols, were resolved by means of pig liver acetone powder (PLAP) and horse liver acetone powder (HLAP).

(R)-(-)-2,2-diphenylcyclopentanol

Denmark, Scott E.,Marcin, Lawrence R.,Schnute, Mark E.,Thorarensen, Atli

, p. 33 - 33 (2017/09/29)

-

New chiral auxiliaries: Their use in the asymmetric hydrogenation of β-acetamidocrotonates

Potin,Dumas,d'Angelo

, p. 3483 - 3486 (2007/10/02)

Synthesis of chiral β-amido esters 7 with high diasteroisomeric excess was achieved by asymmetric hydrogenation (H2/PtO2) of stereogenic β-acetamidocrotonates 6 in which the chirality is present in the alkyl of the ester part. For such a purpose, new efficient chiral auxiliaries such as 2,2-diphenylcyclopentanol (12) and 1,1-diphenyl-3-methyl-2-butanol (13) were developed.

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