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35176-46-6

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35176-46-6 Usage

Chemical Family

Phenols

Structure

Benzene ring with two hydroxyl (OH) groups at the 1 and 3 positions

Functional Group

Nonadecyl functional group attached to the benzene ring

Terminology

Nonadecyl-terminated hydroxybenzene

Applications

Intermediate in the production of surfactants and emulsifiers

Applications

Synthesis of organic compounds

Potential Properties

Antioxidant and antimicrobial properties

Field of Interest

Chemical research and development

Check Digit Verification of cas no

The CAS Registry Mumber 35176-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,7 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35176-46:
(7*3)+(6*5)+(5*1)+(4*7)+(3*6)+(2*4)+(1*6)=116
116 % 10 = 6
So 35176-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C25H44O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23-20-24(26)22-25(27)21-23/h20-22,26-27H,2-19H2,1H3

35176-46-6 Well-known Company Product Price

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  • Sigma-Aldrich

  • (57981)  5-Nonadecylresorcinol  analytical standard

  • 35176-46-6

  • 57981-10MG

  • 6,686.55CNY

  • Detail

35176-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nonadecylbenzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Benzenediol,5-nonadecyl

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:35176-46-6 SDS

35176-46-6Relevant articles and documents

Cereal grain resorcinolic lipids: mono and dienoic homologues are present in rye grains

Kozubek, Arkadiusz,Tyman, John H. P.

, p. 29 - 36 (2007/10/03)

Analyses (UV, IR, 1H-NMR, MS) of the main phenolic fraction isolated by sequential separation on normal-phase and argentation chromatography on silica gel confirmed the presence of monoenoic and dienoic homologues of 1,3-dihydroxy-5-n-alkylbenzene in acet

A cytotoxic constituent of Lysimachia japonica THUNB. (Primulaceae) and the structure-activity relationships of related compounds

Arisawa,Ohmura,Kobayashi,Morita

, p. 2431 - 2434 (2007/10/02)

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