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90110-98-8

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90110-98-8 Usage

General Description

2-Bromo-4-cyanobenzyl alcohol is a chemical compound with the molecular formula C8H6BrNO, and it is also known by the chemical name 4-(2-bromo-4-hydroxyphenyl)cyanobenzene. This white crystalline solid is used as a reagent in various chemical reactions and synthesis processes. It is commonly used in the pharmaceutical industry as a building block for the production of certain drugs and as an intermediate in the manufacture of other organic compounds. Additionally, it has applications in the field of organic chemistry for its ability to undergo various reactions, such as substitution and addition reactions, making it a versatile compound in laboratory settings. However, 2-Bromo-4-cyanobenzyl alcohol should be handled with care due to its potential hazards, including skin and eye irritation, and it should be used in a well-ventilated area with proper personal protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 90110-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90110-98:
(7*9)+(6*0)+(5*1)+(4*1)+(3*0)+(2*9)+(1*8)=98
98 % 10 = 8
So 90110-98-8 is a valid CAS Registry Number.

90110-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-4-(hydroxymethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names 3-bromo-4-(hydroxymethyl)benzonitrile

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:90110-98-8 SDS

90110-98-8Relevant articles and documents

PROTECTIVE GROUPS AND METHODS FOR PROTECTING BENZOXABOROLES OR OXABOROLES

-

, (2019/10/01)

The present invention relates in part protective groups that can be used to reversibly protect benzoxaboroles and/or oxaboroles and yield the corresponding protected complexes. The invention further relates to the use of these protective groups to protect benzoxaboroles and/or oxaboroles.

A general method for selective recognition of monosaccharides and oligosaccharides in water

Gunasekara, Roshan W.,Zhao, Yan

, p. 829 - 835 (2017/05/17)

Molecular recognition of carbohydrates plays vital roles in biology but has been difficult to achieve with synthetic receptors. Through covalent imprinting of carbohydrates in boroxole-functionalized cross-linked micelles, we prepared nanoparticle receptors for a wide variety of mono- and oligosaccharides. The boroxole functional monomer bound the sugar templates through cis-1,2-diol, cis-3,4-diol, and trans-4,6-diol. The protein-sized nanoparticles showed excellent selectivity for daldohexoses in water with submillimolar binding affinities and completely distinguished the three biologically important hexoses (glucose, mannose, and galactose). Glycosides with nonpolar aglycon showed stronger binding due to enhanced hydrophobic interactions. Oligosaccharides were distinguished on the basis of their monosaccharide building blocks, glycosidic linkages, chain length, as well as additional functional groups that could interact with the nanoparticles.

2-ARYL SELENAZOLE COMPOUND AND PHARMACEUTICAL COMPOSITION THEREOF

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, (2015/11/16)

Disclosed are a 2-aryl selenazole compound and a pharmaceutical composition thereof, where the 2-aryl selenazole compound is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof. The 2-aryl selenazole compound has the activi

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