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155268-88-5

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155268-88-5 Usage

General Description

"(4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine" is a chemical compound that contains the elements boron, oxygen, carbon, and hydrogen. It is a chiral oxazaborolidine, meaning it has a specific three-dimensional arrangement of atoms that gives it a unique chemical and biological activity. (4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine is often used as a catalyst in organic synthesis, particularly in asymmetric transformations, meaning it can facilitate chemical reactions in a way that produces only one of two possible mirror-image molecules. Its structure and properties make it useful in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The "4R" designation indicates the stereochemistry at the fourth carbon atom, further specifying its three-dimensional arrangement.

Check Digit Verification of cas no

The CAS Registry Mumber 155268-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,6 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155268-88:
(8*1)+(7*5)+(6*5)+(5*2)+(4*6)+(3*8)+(2*8)+(1*8)=155
155 % 10 = 5
So 155268-88-5 is a valid CAS Registry Number.

155268-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine

1.2 Other means of identification

Product number -
Other names (R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine

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:155268-88-5 SDS

155268-88-5Downstream Products

155268-88-5Relevant articles and documents

A total synthesis of galbonolide B

Parsons, Philip J.,Pennicott, Lewis,Eshelby, James,Goessman, Matthias,Highton, Adrian,Hitchcock, Peter

, p. 9387 - 9390 (2007)

(Chemical Equation Presented) An ester enolate rearrangement/silicon mediated fragmentation cascade was used to convert 7 and 8 into the alcohol 9. The alcohol 9 was converted into the allylic alcohol 12 and then to the ester 14. A further ester enolate r

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