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133914-73-5

133914-73-5

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133914-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133914-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133914-73:
(8*1)+(7*3)+(6*3)+(5*9)+(4*1)+(3*4)+(2*7)+(1*3)=125
125 % 10 = 5
So 133914-73-5 is a valid CAS Registry Number.

133914-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-dimethylaminomethyl-3-hydroxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 5-acetamido-2-[(N,N-dimethylamino)methyl]-phenol

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:133914-73-5 SDS

133914-73-5Downstream Products

133914-73-5Relevant articles and documents

Isoquine and Related Amodiaquine Analogues: A New Generation of Improved 4-Aminoquinoline Antimalarials

O'Neill, Paul M.,Mukhtar, Amira,Stocks, Paul A.,Randle, Laura E.,Hindley, Stephen,Ward, Stephen A.,Storr, Richard C.,Bickley, Jamie F.,O'Neil, Ian A.,Maggs, James L.,Hughes, Ruth H.,Winstanley, Peter A.,Bray, Patrick G.,Park, B. Kevin

, p. 4933 - 4945 (2007/10/03)

Amodiaquine (AQ) (2) is a 4-aminoquinoline antimalarial that can cause adverse side effects including agranulocytosis and liver damage. The observed drug toxicity is believed to involve the formation of an electrophilic metabolite, amodiaquine quinoneimin

Organic synthesis

-

, (2008/06/13)

The conversion of ortho-hydroxylated Mannich bases to the corresponding methylated compounds, e.g., cresols, can be effectively carried out using a novel hydrogenation technique.

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