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1-Naphthalenecarbonyl chloride, 5-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101665-68-3

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101665-68-3 Usage

Synonym

1-Acetyl-5-methylnaphthalene

Appearance

Yellowish liquid

Odor

Strong, pungent

Use

Intermediate in the production of pharmaceuticals, dyes, and agrochemicals

Reactivity

Highly reactive

Handling precautions

Should be handled with caution

Main applications

Building block in the synthesis of various chemical compounds, reagent in organic chemistry reactions

Other uses

Flavoring agent in the food industry, fragrance in the cosmetic industry

Check Digit Verification of cas no

The CAS Registry Mumber 101665-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,6 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101665-68:
(8*1)+(7*0)+(6*1)+(5*6)+(4*6)+(3*5)+(2*6)+(1*8)=103
103 % 10 = 3
So 101665-68-3 is a valid CAS Registry Number.

101665-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylnaphthalene-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 5-Methyl-1-naphthoylchloride

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:101665-68-3 SDS

101665-68-3Relevant academic research and scientific papers

Delineating noncovalent interactions between the azinomycins and double-stranded DNA: Importance of the naphthalene substitution pattern on interstrand cross-linking efficiency

Landreau, Cyrille A. S.,LePla, Rachel C.,Shipman, Michael,Slawin, Alexandra M. Z.,Hartley, John A.

, p. 3505 - 3507 (2007/10/03)

(Chemical Equation Presented) Using a series of synthetic azinomycin analogues, it is shown that the efficiency of in vitro DNA interstrand cross-linking is markedly reduced when either the C-5′ methyl group or both the C-5′ methyl and C-3′ methoxy groups

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