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92632-84-3

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92632-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92632-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92632-84:
(7*9)+(6*2)+(5*6)+(4*3)+(3*2)+(2*8)+(1*4)=143
143 % 10 = 3
So 92632-84-3 is a valid CAS Registry Number.

92632-84-3SDS

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 (E)-6-benzoyloxy-4-methyl-2-hexen-1-ol

1.2 Other means of identification

Product number -
Other names Benzoic acid (E)-6-hydroxy-3-methyl-hex-2-enyl ester

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:92632-84-3 SDS

92632-84-3Downstream Products

92632-84-3Relevant articles and documents

Chiral Amino Alcohol Accelerated and Stereocontrolled Allylboration of Iminoisatins: Highly Efficient Construction of Adjacent Quaternary Stereogenic Centers

Tan, Qiuyuan,Wang, Xinqiao,Xiong, Yang,Zhao, Zimeng,Li, Lu,Tang, Pei,Zhang, Min

supporting information, p. 4829 - 4833 (2017/04/11)

We have developed a highly efficient asymmetric allylboration of ketimines with nonchiral γ,γ-disubstituted allylboronic acids by using a chiral amino alcohol as the directing group, which is otherwise challenging. The amino alcohol not only serves as a cheap source of nitrogen and chirality, but also dramatically enhances the reactivity. The versatility of this method was demonstrated by its ability to access all four stereoisomers with adjacent quaternary carbon centers. A reaction model was proposed to explain the diastereoselectivity and the rate-accelerating effect.

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