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2H-1-Benzopyran-2-one, 6-bromo-4-(diazomethyl)-7-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

272107-65-0

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272107-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 272107-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,1,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 272107-65:
(8*2)+(7*7)+(6*2)+(5*1)+(4*0)+(3*7)+(2*6)+(1*5)=120
120 % 10 = 0
So 272107-65-0 is a valid CAS Registry Number.

272107-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-4-(diazoniomethylidene)-2-hydroxychromen-7-olate

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran-2-one,6-bromo-4-(diazomethyl)-7-hydroxy

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:272107-65-0 SDS

272107-65-0Downstream Products

272107-65-0Relevant academic research and scientific papers

Photoregulation of thrombin aptamer activity using Bhc caging strategy

Li, YiMing,Shi, Jing,Luo, ZhaoFeng,Jiang, Hao,Chen, XiaoYun,Wang, FengLiang,Wu, Xu,Guo, QingXiang

supporting information; experimental part, p. 5368 - 5371 (2010/08/19)

Thrombin aptamer was attempted to cage with Bhc (6-bromo-7-hydroxycoumarin-4-ylmethyl) group for controlling its specific affinity to target molecular through photolysis. By multiple-caging strategy, aptamer could be rendered biologically inert and partia

PROTECTING GROUPS WITH INCREASED PHOTOSENSITIVITIES

-

, (2008/06/13)

Protecting groups derived from a halogenated coumarin group, a quinoline-2-one group, a xanthene group, a thioxanthene group, a selenoxanthene group, or an anthracene group are described. The protecting groups is photolabile and can be removed by irradiating the group with light, such as flash photolysis with ultraviolet radiation or pulsed infrared radiation.

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