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126577-48-8

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126577-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126577-48-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,7 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126577-48:
(8*1)+(7*2)+(6*6)+(5*5)+(4*7)+(3*7)+(2*4)+(1*8)=148
148 % 10 = 8
So 126577-48-8 is a valid CAS Registry Number.

126577-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-1,1-diphenyl-1,2-propanediol

1.2 Other means of identification

Product number -
Other names (R)-1,1-Diphenyl-propane-1,2-diol

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:126577-48-8 SDS

126577-48-8Upstream product

126577-48-8Relevant articles and documents

Enantio- and Diastereoselective 1,2-Additions to α-Ketoesters with Diborylmethane and Substituted 1,1-Diborylalkanes

Murray, Stephanie A.,Green, Jacob C.,Tailor, Sanita B.,Meek, Simon J.

supporting information, p. 9065 - 9069 (2016/07/26)

The catalytic enantioselective synthesis of boronate-substituted tertiary alcohols through additions of diborylmethane and substituted 1,1-diborylalkanes to α-ketoesters is reported. The reactions are catalyzed by readily available chiral phosphine/copper(I) complexes and produce β-hydroxyboronates containing up to two contiguous stereogenic centers in up to 99:1 e.r. and greater than 20:1 d.r. The utility of the organoboron products is demonstrated through several chemoselective functionalizations. Evidence indicates the reactions occur via an enantioenriched α-boryl-copper-alkyl intermediate.

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