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106575-40-0

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106575-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106575-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,7 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106575-40:
(8*1)+(7*0)+(6*6)+(5*5)+(4*7)+(3*5)+(2*4)+(1*0)=120
120 % 10 = 0
So 106575-40-0 is a valid CAS Registry Number.

106575-40-0SDS

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 7-phenyl-3-heptyn-2-ol

1.2 Other means of identification

Product number -
Other names -

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:106575-40-0 SDS

106575-40-0Relevant articles and documents

Stereoselective Alkyne Hydrohalogenation by Trapping of Transfer Hydrogenation Intermediates

Das, Manas,Kaicharla, Trinadh,Teichert, Johannes F.

supporting information, p. 4926 - 4929 (2018/08/24)

A catalytically generated vinylcopper complex, the reactive intermediate of a copper(I)-catalyzed alkyne transfer hydrogenation, can be trapped by commercially available halogen electrophiles. In this manner, internal alkynes can stereoselectively be hydrohalogenated to the corresponding vinyl chlorides, bromides, and iodides.

Directing group-controlled hydrosilylation: Regioselective functionalization of alkyne

Kawasaki, Yuuya,Ishikawa, Youhei,Igawa, Kazunobu,Tomooka, Katsuhiko

supporting information; experimental part, p. 20712 - 20715 (2012/02/15)

Pt(0)-catalyzed hydrosilylation of unsymmetric alkynes proceeds in a highly regioselective manner with a dimethylvinylsilyl (DMVS) group as the directing group. This hydrosilylation affords a single regioisomer of silylalkenes from propargylic and homopro

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