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3-Buten-2-one, 4-benzo[b]thien-5-yl-, (3E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329768-76-5

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329768-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329768-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,7,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 329768-76:
(8*3)+(7*2)+(6*9)+(5*7)+(4*6)+(3*8)+(2*7)+(1*6)=195
195 % 10 = 5
So 329768-76-5 is a valid CAS Registry Number.

329768-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-(benzo[b]thiophen-5-yl)-but-3-en-2-one

1.2 Other means of identification

Product number -
Other names 1-(benzo[b]thien-5-yl)but-1-en-3-one

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:329768-76-5 SDS

329768-76-5Downstream Products

329768-76-5Relevant academic research and scientific papers

Substituent dependent photochemical rearrangements of halostyrylheterocycles in acid media

Ho, Jinn-Hsuan,Ho, Tong-Ing

, p. 4669 - 4672 (2003)

New photorearrangement product 2 and hydrolysis product 3 are obtained by irradiating acidic halostyrylheterocycles 1a-f. The competing formal [1,3]hydrogen shift and ring opening of dihydrophenanthrene intermediate is responsible for the product formatio

A family of stilbene-ethers as photolabile protecting groups for primary alcohols offers controlled deprotection based on choice of wavelength

Ho, Jinn-Hsuan,Lee, Ya-Wen,Chen, Ying-Zhe,Chen, Pin-Sian,Liu, Wei-Qi,Ding, Yi-Shun

, p. 7325 - 7332 (2013/08/23)

A novel stilbene-ether type of photolabile protecting group (PPG) for hydroxyl group has been developed. It contains a stable aryl ether group in the protected form and can be deprotected by acid-catalyzed photorearrangement under 300-nm irradiation. The selective deprotection has also been achieved by irradiation of the mixture of 4-alkoxystilbene and 2-(4-alkoxystyryl)furan at 365 nm.

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