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49818-48-6

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49818-48-6 Usage

Chemical composition

Contains benzene, methoxy, and nitro functional groups.

Usage

Used as a fragrance ingredient in cosmetics and personal care products, as well as a flavoring agent in food products.

Importance

Enhances the sensory experience of fragranced and flavored products.

Safety considerations

Should be used in controlled amounts to avoid potential adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 49818-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,1 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 49818-48:
(7*4)+(6*9)+(5*8)+(4*1)+(3*8)+(2*4)+(1*8)=166
166 % 10 = 6
So 49818-48-6 is a valid CAS Registry Number.

49818-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-3-[(E)-2-nitroethenyl]-2-phenylmethoxybenzene

1.2 Other means of identification

Product number -
Other names 2-Benzyloxy-3-methoxynitrostyrol

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:49818-48-6 SDS

49818-48-6Relevant articles and documents

Benzo aza compound, preparation method and use thereof

-

Paragraph 0099; 0100, (2017/08/22)

Belonging to the field of pharmaceutical chemistry, the invention relates to a benzoazepine compound, a preparation method and application thereof, in particular to the benzoazepine compound, its preparation method and application in the field of treatment of nervous system diseases, especially application in the field of drug addiction related to dopamine D1 and D3 receptors. The benzoazepine compound and pharmacologically acceptable inorganic or organic salts thereof have a structure shown as formula (I). Results of drug experiments carried out by the invention show that the benzoazepine compound and its pharmacologically acceptable inorganic or organic salts have high antagonistic activity on dopamine D1 and D3, can be used as drug leads for further development of dopamine receptor antagonists with good selectivity and high activity, and can be used as potential drugs for treatment of drug addiction by dopamine D1, D3 receptor antagonists. (formula (I)).

A facile synthesis of 1-alkyl-5-arylalkoxy-6-methoxy-3,4- dihydroisoquinolines

Yim, Heong-Seup,Kim, Ho-Kyun,Kim, Jeum-Jong,Kweon, Deok-Heon,Lee, Sang-Gyeong,Kim, Jung-Ho,Yoon, Yong-Jin

, p. 909 - 914 (2008/04/05)

(Chemical Equation Presented) 1-Alkyl-5-arylalkoxy-6-methoxy-3,4- dihydroisoquinolines were synthesized by the alkylation of 1-alkyl-5-hydroxy-6- methoxy-3,4-dihydroisoquinolines with arylalkyl halide in the presence of potassium carbonate. 1-Alkyl-5-hydroxy-6-methoxy-3,4-dihydroisoquinolines as key precursor prepared from o-vaniline via 6 steps.

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