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Benzoyl chloride, 2-(hexyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54464-32-3

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54464-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54464-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,6 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54464-32:
(7*5)+(6*4)+(5*4)+(4*6)+(3*4)+(2*3)+(1*2)=123
123 % 10 = 3
So 54464-32-3 is a valid CAS Registry Number.

54464-32-3SDS

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 2-hexoxybenzoyl chloride

1.2 Other means of identification

Product number -
Other names hexyloxybenzoyl chloride

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:54464-32-3 SDS

54464-32-3Upstream product

54464-32-3Relevant academic research and scientific papers

Synthesis and structure-activity relationship of dehydroxymethylepoxyquinomicin analogues as inhibitors of NF-κB functions

Chaicharoenpong, Chanya,Kato, Kuniki,Umezawa, Kazuo

, p. 3933 - 3939 (2002)

We previously found dehydroxymethylepoxyquinomicin (DHMEQ) inhibited NF-κB activation and showed anti-inflammatory activity in vivo. Here we designed and synthesized analogues of DHMEQ and tested their biological activity as NF-κB inhibitors in human T cell leukemia Jurkat cells. The hydroxyl group at the 2-position of the benzamide moiety was found to be essential for the inhibitory activity. But etherification of this group did not diminish the activity completely. Thus, for further mechanistic studies the hydroxyl group at the 2-position may be useful for extension with a linker and biotin moiety.

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