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63955-87-3

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63955-87-3 Usage

Chemical Family

Amines

Derivation

Derived from 3,4-dimethylphenol and diethylethanolamine

+ Antihistamine

It can reduce or prevent histamine effects in the body.

+ Anticholinergic

It can inhibit the action of acetylcholine, a neurotransmitter.

+ Sedative

It can help to reduce excitement or calm the user.

+ Antipruritic

It can relieve itching or a rash with a burning or stinging sensation.

+ Pharmaceutical Products

Used as an ingredient in antihistamine medications.

+ Agricultural Products

Used as a pesticide and insecticide to control pests and insects.

Check Digit Verification of cas no

The CAS Registry Mumber 63955-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,5 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63955-87:
(7*6)+(6*3)+(5*9)+(4*5)+(3*5)+(2*8)+(1*7)=163
163 % 10 = 3
So 63955-87-3 is a valid CAS Registry Number.

63955-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dimethylphenoxy)-N,N-diethylethanamine

1.2 Other means of identification

Product number -
Other names -

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:63955-87-3 SDS

63955-87-3Relevant articles and documents

Synthesis of the Sesquiterpene (+/-)-Lemnal-5a-en-2-one

Dischmann, Michael,Ernst, Ludger,Wolf, Herbert

, p. 727 - 738 (2007/10/02)

SnCl4-catalysed cyclization of the carboxylic acid 4 stereoselectively gives the tricyclus 5.This cyclization is the key reaction in the synthesis of lemnal-5a-en-2-one .As a model compound the carboxylic acid 2 was cyclized to yield 3. 2 and 4 w

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