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100379-06-4

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100379-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100379-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100379-06:
(8*1)+(7*0)+(6*0)+(5*3)+(4*7)+(3*9)+(2*0)+(1*6)=84
84 % 10 = 4
So 100379-06-4 is a valid CAS Registry Number.

100379-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-methylhept-6-en-3-yn-2-ol

1.2 Other means of identification

Product number -
Other names 6-Hepten-3-yn-2-ol,6-bromo-2-methyl

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:100379-06-4 SDS

100379-06-4Downstream Products

100379-06-4Relevant articles and documents

Au(I)-Catalyzed Cyclization/Semipinacol Rearrangement Reaction of Allenes to Construct Quaternary Carbon-Containing Scaffolds

Zheng, Tian-Lu,Zhang, Ye,Gou, A-Long,Cheng, Fu,Liu, Si-Zhan,Yu, Lan,Cui, Ming-Yue,Xu, Xue-Tao,Zhang, Kun,Wang, Shao-Hua

, p. 7073 - 7077 (2020)

The development of methods toward the construction of quaternary carbon centers has been a hot topic in recent years. In this work, an Au(I)-catalyzed intramolecular cyclization/semipinacol rearrangement of allene-containing allylic silyl ether was developed to provide a direct strategy for the construction of multisubstituted cyclohexene-type compounds with a quaternary carbon center in moderate to good yields. In particular, this method provides an alternative synthetic strategy for the construction of a multisubstituted spirocyclo[4.5]decane skeleton and may be applied to the synthesis of related bioactive molecules and their derivatives, thus facilitating the corresponding functional studies.

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