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134594-22-2

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134594-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134594-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,9 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134594-22:
(8*1)+(7*3)+(6*4)+(5*5)+(4*9)+(3*4)+(2*2)+(1*2)=132
132 % 10 = 2
So 134594-22-2 is a valid CAS Registry Number.

134594-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxynaphthalene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-Naphthalenecarboxaldehyde,5-methoxy

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:134594-22-2 SDS

134594-22-2Downstream Products

134594-22-2Relevant articles and documents

BICYCLIC ARYL AND HETEROARYL COMPOUNDS FOR THE TREATMENT OF METABOLIC DISORDERS

-

Page/Page column 26, (2009/01/20)

Compounds of formula (I): or pharmaceutically acceptable salts thereof, are opioid receptor modulators, e.g. mu- opioid receptor antagonists, neutral antagonists or inverse agonists, and are useful for the treatment of metabolic disorders including obesity.

Regioselectivity in the Reactions of Methoxydehydrobenzenes with Furans. Part 1. Reactions of 3-Methoxydehydrobenzene and 3-(Methoxycarbonyl)dehydrobenzene with 2-Substituted Furans.

Giles, Robin G. F.,Sargent, Melvyn V.,Sianipar, Hercules

, p. 1571 - 1579 (2007/10/02)

The isomer ratios for the cycloadducts obtained for the reaction of 3-methoxydehydrobenzene, generated from 2-amino-6-methoxybenzoic acid by aprotic diazotization, or from 2-bromo-3-methoxyphenyl toluene-p-sulphonate by treatment with butyllithium, and fo

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