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57322-44-8

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57322-44-8 Usage

General Description

(1-METHYLNAPHTHALEN-4-YL)METHANOL is a chemical compound with the molecular formula C11H12O. It is primarily used as a building block in organic synthesis and can be used as an intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. (1-METHYLNAPHTHALEN-4-YL)METHANOL is a derivative of naphthylmethanol and possesses a naphthalene ring with a methyl group attached to the fourth carbon, along with a hydroxyl group. It may also have potential uses in the manufacturing of fragrances and flavors due to its aromatic properties. Additionally, it is important to handle this chemical with caution as it may pose health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 57322-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,2 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57322-44:
(7*5)+(6*7)+(5*3)+(4*2)+(3*2)+(2*4)+(1*4)=118
118 % 10 = 8
So 57322-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O/c1-9-6-7-10(8-13)12-5-3-2-4-11(9)12/h2-7,13H,8H2,1H3

57322-44-8SDS

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 (4-methylnaphthalen-1-yl)methanol

1.2 Other means of identification

Product number -
Other names 11-Oxy-1.4-dimethyl-naphthalin

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:57322-44-8 SDS

57322-44-8Relevant articles and documents

Controlled photochemical release of nitric oxide from O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates

Bushan, K. Mani,Xu, Hua,Ruane, Patrick H.,D'Sa, Raechelle A.,Pavlos, Christopher M.,Smith, Joseph A.,Celius, Tevye C.,Toscano, John P.

, p. 12640 - 12641 (2007/10/03)

The photochemistry of O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates has been investigated. Electron-donating methoxy group substitution is shown to have a significant effect on the observed photochemistry, with the appropriate substitution pattern resulting in efficient diazeniumdiolate photorelease. Observed nitric oxide release rates from these photoprecursors are consistent with those expected for normal thermal dissociation of the diazeniumdiolate in aqueous solutions and show the same pH dependence. Copyright

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