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216755-56-5

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216755-56-5 Usage

General Description

3-Bromo-5-fluorobenzyl alcohol is a chemical compound with the molecular formula C7H6BrFO. It is an organic compound that contains a benzyl alcohol group, a bromine atom, and a fluorine atom, making it a derivative of benzyl alcohol. It is commonly used as a reagent in organic synthesis, and its properties make it a valuable intermediate in the production of pharmaceuticals and agrochemicals. The compound has a wide range of applications in the chemical industry and is known for its ability to undergo various chemical reactions, making it useful in the synthesis of diverse organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 216755-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,7,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 216755-56:
(8*2)+(7*1)+(6*6)+(5*7)+(4*5)+(3*5)+(2*5)+(1*6)=145
145 % 10 = 5
So 216755-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NO/c1-12-5-2-3-6(11-4-5)7(8,9)10/h2-4H,1H3

216755-56-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H61415)  3-Bromo-5-fluorobenzyl alcohol, 98%   

  • 216755-56-5

  • 250mg

  • 243.0CNY

  • Detail
  • Alfa Aesar

  • (H61415)  3-Bromo-5-fluorobenzyl alcohol, 98%   

  • 216755-56-5

  • 1g

  • 732.0CNY

  • Detail
  • Alfa Aesar

  • (H61415)  3-Bromo-5-fluorobenzyl alcohol, 98%   

  • 216755-56-5

  • 5g

  • 2926.0CNY

  • Detail

216755-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-bromo-5-fluorophenyl)methanol

1.2 Other means of identification

Product number -
Other names (3-bromo-5-fluoro-phenyl)-methanol

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:216755-56-5 SDS

216755-56-5Relevant articles and documents

AZOLE-SUBSTITUTED PYRIDINE COMPOUND

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Paragraph 0691; 0692, (2019/01/08)

The present invention provides a compound represented by formula [I'| shown below or a pharmaceutically acceptable salt thereof that has an inhibitory effect on 20-HETE producing enzyme, wherein the structure represented by formula [III] shown below represents any of the structures represented by formula group [IV] shown below, wherein R1 represents a hydrogen atom, a fluorine atom, methyl, etc.; R2, R3, and R4 each independently represent a hydrogen atom, a fluorine atom, or methyl; W represents a single bond, C1-3alkanediyl, or the formula -O-CH2CH2-; and ring A represents (a) substituted C4-6cycloalkyl, (b) substituted 4- to 6-membered saturated nitrogen-containing heterocyclyl, (c) substituted phenyl, (d) substituted pyridyl, (e) substituted 2,3-dihydrobenzofuran, (f) 4- to 6-membered saturated oxygen-containing heterocyclyl, etc.

SUBSTITUTED AROMATIC COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF OSTEOPOROSIS

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Paragraph 00127, (2016/05/02)

The present invention concerns the use of compounds for preventing and/or treating osteoporosis, for stimulating bone formation, for stimulating bone remodeling, for stimulating the differentiation and mineralization of osteoblasts, for inhibiting bone resorption and for modulating serum level of adiponectin in a subject. These uses have been found for compounds represented by Formula I and pharmaceutically acceptable salts thereof. wherein A is C5 alkyl, C6 alkyl, C5 alkenyl, C6 alkenyl, C(O)-(CH2)n-CH3 or CH(OH)-(CH2)n-CH3 wherein n is 3 or 4; R1 is H, F or OH; R2 is H, F, OH, C6 alkyl, C5 alkenyl, C6 alkenyl, C(O)-(CH2)n-CH3 or CH(OH)-(CH2)n-CH3 wherein n is 3 or 4; R3 is H, F, OH or CH2Ph; R4 is H, F, or OH; Q is 1) (CH2)mC(O)OH wherein m is 1 or 2, 2) CH(F)-C(O)OH, 3) CF2-C(O)OH or 4) C(O)-C(O)OH.

Aminoheteroaryl benzamides as kinase inhibitors

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Page/Page column 271; 272, (2016/02/15)

The present invention provides a compound of Formula (I) or a salt thereof; and therapeutic uses of these compounds. The present invention further provides pharmaceutical compositions comprising these compounds, and compositions comprising these compounds with a therapeutic co-agent.

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