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4-Pentenethioamide, N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81114-06-9

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81114-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81114-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81114-06:
(7*8)+(6*1)+(5*1)+(4*1)+(3*4)+(2*0)+(1*6)=89
89 % 10 = 9
So 81114-06-9 is a valid CAS Registry Number.

81114-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylpent-4-enethioamide

1.2 Other means of identification

Product number -
Other names N-phenyl 4-pentenethioamide

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:81114-06-9 SDS

81114-06-9Relevant academic research and scientific papers

IODINE-INDUCED IMINOTHIOLACTONIZATION OF γ,δ-UNSATURATED SECONDARY THIOAMIDES, NEW ENTRY TO 2-ACETOAMIDOTHIOPHENES

Takahata, Hiroki,Suzuki, Toshiaki,Maruyama, Mihoko,Moriyama, Keiko,Mozumi, Mayumi,et.al.

, p. 4777 - 4786 (2007/10/02)

Iodine-induced cyclization of γ,δ-unsaturated secondary thioamides 1 proceeded regio- (5-exo-trigonal) and chemo- (sulfur-carbon bond formation)selectively, providing iminothiolactones 2, which were converted in two-step sequences (dehydroiodination and N-acetylation) into 2-acetoamidothiophenes 4.This procedure was performed in one flask to afford polysubstituted 2-aminothiophenes.

THE REGIOSELECTIVE SC AND SN ALLYLIC REARRANGEMENT OF S-ALLYLTHIOIMIDATE

Tamaru, Y.,Kagotani, M.,Yoshida, Z.

, p. 4245 - 4248 (2007/10/02)

The radioselective SC and SN allylic rearrangements of S-allylthioimidates are realized by thermolysis (160-200 deg C) or palladium (II) catalysis (1-10 molpercent in refluxing THF), respectively.

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