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123239-65-6

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123239-65-6 Usage

General Description

(4-Methoxynaphthalen-2-yl)(phenyl)Methanol is a chemical compound that belongs to the class of organic compounds known as naphthalenes. It is a white crystalline powder with a molecular formula of C19H16O2 and a molecular weight of 280.33 g/mol. (4-Methoxynaphthalen-2-yl)(phenyl)Methanol is primarily used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It possesses aromatic and phenolic properties, making it useful in various chemical reactions and processes. However, it is important to handle and use this compound with caution, as it may be harmful if ingested, inhaled, or absorbed through the skin, and it may also cause irritation to the eyes and skin.

Check Digit Verification of cas no

The CAS Registry Mumber 123239-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,3 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123239-65:
(8*1)+(7*2)+(6*3)+(5*2)+(4*3)+(3*9)+(2*6)+(1*5)=106
106 % 10 = 6
So 123239-65-6 is a valid CAS Registry Number.

123239-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxynaphthalen-2-yl)-phenylmethanol

1.2 Other means of identification

Product number -
Other names (4-Methoxynaphthalen-2-yl)(phenyl)methanol

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:123239-65-6 SDS

123239-65-6Relevant articles and documents

2-Substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity

Batt,Maynard,Petraitis,Shaw,Galbraith,Harris

, p. 360 - 370 (2007/10/02)

The synthesis, biological evaluation, and structure-activity relationships of a series of 1-naphthols bearing carbon substituents at the 2-position are described. These compounds are potent inhibitors of the 5-lipoxygenase from RBL-1 cells and also inhibi

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