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54896-65-0

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54896-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54896-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,9 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54896-65:
(7*5)+(6*4)+(5*8)+(4*9)+(3*6)+(2*6)+(1*5)=170
170 % 10 = 0
So 54896-65-0 is a valid CAS Registry Number.

54896-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbamoyl-DL-tyrosine

1.2 Other means of identification

Product number -
Other names N-Carbamoyl-DL-tyrosin

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:54896-65-0 SDS

54896-65-0Relevant articles and documents

A practically simple, catalyst free and scalable synthesis of: N -substituted ureas in water

Tiwari, Lata,Kumar, Varun,Kumar, Bhuvesh,Mahajan, Dinesh

, p. 21585 - 21595 (2018)

A practically simple, mild and efficient method is developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without organic co-solvent. Using this methodology, a variety of N-substituted ureas (mono-, di- and cyclic-) were synthesized in good to excellent yields with high chemical purity by applying simple filtration or routine extraction procedures avoiding silica gel purification. The developed methodology was also found to be suitable for gram scale synthesis of molecules having commercial application in large volumes. The identified reaction conditions were found to promote a unique substrate selectivity from a mixture of two amines.

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