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3-Butyn-1-ol, 4-(phenylthio)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88695-33-4

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88695-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88695-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,9 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88695-33:
(7*8)+(6*8)+(5*6)+(4*9)+(3*5)+(2*3)+(1*3)=194
194 % 10 = 4
So 88695-33-4 is a valid CAS Registry Number.

88695-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,4-phenylsulfanylbut-3-yn-1-ol

1.2 Other means of identification

Product number -
Other names 3-Butyn-1-ol,4-(phenylthio)-,acetate

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:88695-33-4 SDS

88695-33-4Relevant academic research and scientific papers

Iridium-catalyzed intermolecular azide-alkyne cycloaddition of internal thioalkynes under mild conditions

Ding, Shengtao,Jia, Guochen,Sun, Jianwei

, p. 1877 - 1880 (2014/03/21)

An iridium-catalyzed azide-alkyne cycloaddition reaction (IrAAC) of electron-rich internal alkynes is described. It is the first efficient intermolecular AAC of internal thioalkynes. The reaction exhibits remarkable features, such as high efficiency and r

SILA-PUMMERER REARRANGEMENTS AT SP2-HYBRIDIZED CARBON

Hart, David J.,Tsai, Yeun-Min

, p. 4387 - 4390 (2007/10/02)

α-Trimethylsilylvinyl sulfoxides undergo sila-Pummerer rearrangements upon warming in benzene.Alkynes, vinylsulfoxides, and ketene S,O-acetals are obtained as products.

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