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4242-15-3

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4242-15-3 Usage

General Description

5-Methyl-2-tetralone is a chemical compound with the molecular formula C11H14O. It is a member of the tetralone family, which are bicyclic organic compounds. This particular chemical is a yellow, oily liquid at room temperature and is insoluble in water but soluble in organic solvents. 5-Methyl-2-tetralone is commonly used as a building block in the synthesis of various pharmaceuticals and other organic compounds. It is often employed in research and development laboratories for organic synthesis and medicinal chemistry. This chemical has potential applications in the pharmaceutical and agrochemical industries due to its versatile reactivity and low toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 4242-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4242-15:
(6*4)+(5*2)+(4*4)+(3*2)+(2*1)+(1*5)=63
63 % 10 = 3
So 4242-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O/c1-8-3-2-4-9-7-10(12)5-6-11(8)9/h2-4H,5-7H2,1H3

4242-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 5-Methyl-2-tetralone

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:4242-15-3 SDS

4242-15-3Relevant articles and documents

Regioisomerism in the synthesis of a chiral aminotetralin drug compound: Unraveling mechanistic details and diastereomer-specific in-depth NMR investigations

Schuisky, Peter,Federsel, Hans-Juergen,Tian, Wei

scheme or table, p. 5503 - 5514 (2012/09/07)

During chemical process development of a novel 2-aminotetralin derivative intended for use as an antidepressant, scrutiny of the byproduct present in the drug molecule revealed a set of regioisomers. Detailed studies showed that this impurity issue origin

Structure-activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH2 at the human melanocortin-1 and -4 receptors: Histidine substitution

Cheung, Adrian Wai-Hing,Danho, Waleed,Swistok, Joseph,Qi, Lida,Kurylko, Grazyna,Rowan, Karen,Yeon, Mitch,Franco, Lucia,Chu, Xin-Jie,Chen, Li,Yagaloff, Keith

, p. 133 - 137 (2007/10/03)

Systematic substitution of His6 residue using non-selective hMC4R pentapeptide agonist (Bu-His6-DPhe7-Arg8-Trp9-Gly 10-NH2) as the template led to the identification of Bu-Atcsu

Selective linear peptides with melanocortin-4 receptor (MC4-R) agonist activity

-

, (2008/06/13)

Peptides of formulae I, II and III selectively activate melanocortin-4 (MC-4) receptor activity.

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