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6630-03-1

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6630-03-1 Usage

Type of compound

Organic compound

Primary use

Antihistamine medication

Symptoms relieved

Allergies, hay fever, common cold

Mechanism of action

Blocks the effects of histamine

Additional uses

Sleep aid, relief of mild Parkinsonism symptoms

Classification

Ethanolamine class of antihistamines

Common over-the-counter product

Benadryl

Side effects

Drowsiness, sedation

Safety

Generally well tolerated when used as directed

Check Digit Verification of cas no

The CAS Registry Mumber 6630-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6630-03:
(6*6)+(5*6)+(4*3)+(3*0)+(2*0)+(1*3)=81
81 % 10 = 1
So 6630-03-1 is a valid CAS Registry Number.

6630-03-1SDS

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 2-(diethylaminomethyl)-3,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names 2-[(diethylamino)methyl]-3,6-dimethylphenol

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:6630-03-1 SDS

6630-03-1Downstream Products

6630-03-1Relevant articles and documents

The activation of aminals and aminol ethers by sulfur dioxide and their reactions with electron rich aromatic compounds

Heaney, Harry,Papageorgiou, George,Wilkins, Robert F.

, p. 13361 - 13372 (2007/10/03)

Reactions of bis(dialkylamino)methanes and ethoxydialkylaminomethanes with nucleophilic aromatic heterocycles in the presence of sulfur dioxide result in the formation of the expected Mannich bases in good yields. Reactions of phenols are similarly activated by sulfur dioxide which lead to improved regioselectivity: in particular the reactions of 2,5-dimethylphenol result in the formation of 2-dialkylaminomethyl-3,6-dimethylphenol whereas reaction occurs at the I-position using the classical procedures.

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