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66611-72-1

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66611-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66611-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66611-72:
(7*6)+(6*6)+(5*6)+(4*1)+(3*1)+(2*7)+(1*2)=131
131 % 10 = 1
So 66611-72-1 is a valid CAS Registry Number.

66611-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methyl-2-oxochromen-7-yl)acetamide

1.2 Other means of identification

Product number -
Other names NA-7

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:66611-72-1 SDS

66611-72-1Relevant articles and documents

FORMATION OF OLIGOMERS IN THE IRRADIATION OF 7-DIETHYLAMINO-4-METHYLCOUMARIN IN ETHANOL

Kalmykova, E. A.,Kuznetsova, N.A.,Kaliya, O.L.,Zhigunova, G.A.,Sergeeva, N.D.

, p. 1361 - 1365 (2007/10/02)

In the continuous irradiation of alcoholic solutions of 7-alkylaminocoumarins, oligomers are formed which absorb radiation in the luminescent region of dyes and therefore interfere with the generation of a laser medium.The average molecular weight of the oligomers corresponds with tri- and tetramers.The fractions with higher molecular weights absorb the generated radiation more effectively.The formation of oligomers is observed in oxygen-containing solutions and increases with increase in the dye concentration and degree of conversion.The most likely route for oligomerization seems to be the condensation of the products of the photooxidation of coumarins through the alkylamino group (of amines and amides), and also of acetaldehyde and formaldehyde in a way similar to the formation of amino-aldehyde resins.

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