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73453-46-0

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73453-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73453-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73453-46:
(7*7)+(6*3)+(5*4)+(4*5)+(3*3)+(2*4)+(1*6)=130
130 % 10 = 0
So 73453-46-0 is a valid CAS Registry Number.

73453-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetyl-N,N'-dicyclohexylmalonamide

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:73453-46-0 SDS

73453-46-0Downstream Products

73453-46-0Relevant articles and documents

Reactions of Acetoacetic Ester Blocked Cyclohexyl Isocyanate

Wicks, Zeno W.,Wu, Kuang-Jong

, p. 2446 - 2448 (2007/10/02)

Acetoacetic ester has been widely reported to be a blocking agent for isocyanates.However, we find that only a trace of isocyanate is formed by thermolysis of acetoacetic ester blocked cyclohexyl isocyanate, 1, at 150 deg C and atmospheric pressure.The major portion is unchanged even after 8 h, with some conversion to acetylmalonic ester, 2, and acetyl-N,N'-dicyclohexylmalonamide, 3.Alcoholysis does not yield the "normal" urethane as blocked isocyanates do but rather esters of 1 with some diesters of 2 and smaller amounts of 3.Significant amounts of N-cyclohexylacetamide, N-cyclohexylmalonamate ester, and some N,N'-dicyclohexylmalonamide are also obtained.Aminolysis leads to N-substituted acetamides and N-cyclohexylmalonamate but no substituted ureas, the "normal" products for aminolysis of blocked isocyanates.In the presence of acid catalysts, alcoholysis leads to N-cyclohexylmalonamates with acetate esters as the other product.

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