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Carbamic acid, [2-hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenyl]-, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189032-16-4

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189032-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189032-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,0,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 189032-16:
(8*1)+(7*8)+(6*9)+(5*0)+(4*3)+(3*2)+(2*1)+(1*6)=144
144 % 10 = 4
So 189032-16-4 is a valid CAS Registry Number.

189032-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-Hydroxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-carbamic acid phenyl ester

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:189032-16-4 SDS

189032-16-4Downstream Products

189032-16-4Relevant academic research and scientific papers

Design of photoaffinity reagents for labeling the auxin receptor in maize

Kosemura, Seiji,Emori, Hideyuki,Yamamura, Shosuke,Anai, Toyoaki,Tomita, Kaori,Hasegawa, Koji

, p. 2125 - 2128 (2007/10/03)

In order to isolate the auxin receptor, we have successfully synthesized two analogues of benzoxazolinones with a trifluoromethyldiazirine group as a photoaffinity probe. These compounds inhibited the auxin-induced growth of etiolated Avena coleoptile segments. Photolyses of these compounds in methanol gave intermolecular O-H insertion products in moderate yields, respectively.

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