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132330-98-4

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132330-98-4 Usage

General Description

3-(Benzyloxy)-2-bromopyridine is a specialized chemical compound that belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-membered aromatic heterocycle where one carbon atom is substituted with a nitrogen atom while the other non-carbon atoms are hydrogens. The specific structure of 3-(benzyloxy)-2-bromopyridine includes a bromine atom and a benzyloxy group, which is the benzyl ether of a hydroxy group, attached at the 2nd and 3rd position of the pyridine ring respectively. This chemical is often used as an intermediate in medicinal and chemistry research for the synthesis of more complex compounds. It is commonly sold as a white or off-white crystalline powder.

Check Digit Verification of cas no

The CAS Registry Mumber 132330-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,3 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132330-98:
(8*1)+(7*3)+(6*2)+(5*3)+(4*3)+(3*0)+(2*9)+(1*8)=94
94 % 10 = 4
So 132330-98-4 is a valid CAS Registry Number.

132330-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Benzyloxy)-2-bromopyridine

1.2 Other means of identification

Product number -
Other names 2-bromo-3-phenylmethoxypyridine

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:132330-98-4 SDS

132330-98-4Relevant articles and documents

Dearomatization through Photoredox Hydroarylation: Discovery of a Radical-Polar Crossover Strategy

Jui, Nathan T.,McDaniel, Kelly A.

, p. 5576 - 5580 (2021)

Indole dearomatization has been achieved via radical hydroarylation. Under mild photoredox conditions, a range of indole derivatives undergo hydroarylation to form 2-arylindoline products. Mechanistically, radical termination occurs primarily via stepwise

NOVEL PIPERIDINE DERIVATIVE

-

Page/Page column 45-46, (2008/06/13)

The invention provides a compound of the following formula (1): wherein m, n, and p are independently an integer of 0 - 4, provided 3 ≤ m + n ≤ 8; X is nitrogen atom or a group of the formula: C-R15; Y is a substituted or unsubstituted aromatic group, etc.; R15, R1, R2, R3, R4 , R5, R6 and R7 are hydrogen atom, a substituted or unsubstituted alkyl group, etc.; and Z is hydrogen atom, cyano group, etc., or a prodrug thereof, or a pharmaceutically acceptable salt thereof, which exhibits an action for enhancing LDL receptor expression, and is useful as a medicament for treating hyperlipidemia, atherosclerosis, etc.

Pyrrolo[2,1,5-cd]indolizine derivatives useful in the prevention or treatment of estrogen related diseases or syndromes

-

, (2008/06/13)

The present invention relates to therapeutically active compounds of formula I a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in the prevention or treatment of estrogen related diseases or syndromes.

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