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78533-68-3

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78533-68-3 Usage

Chemical compound

2-Amino-5-phenyl-1,4,5,6-tetrahydropyrimidine

Classification

Pyrimidine

Structure

Heterocyclic organic compound containing a pyrimidine ring with a phenyl substituent at the 5-position

Applications

1. Pharmaceuticals: Can be used as a building block for the synthesis of other compounds, and in medicinal chemistry for drug discovery and development
2. Potential candidate for the development of new drugs with various biological activities
3. Other potential applications in areas such as materials science and chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 78533-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,3 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78533-68:
(7*7)+(6*8)+(5*5)+(4*3)+(3*3)+(2*6)+(1*8)=163
163 % 10 = 3
So 78533-68-3 is a valid CAS Registry Number.

78533-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-phenyl-1,4,5,6-tetrahydropyrimidine

1.2 Other means of identification

Product number -
Other names 5-Phenyl-1,4,5,6-tetrahydro-pyrimidin-2-ylamine

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:78533-68-3 SDS

78533-68-3Downstream Products

78533-68-3Relevant articles and documents

A facile reduction of 2-aminopyrimidines with triethylsilane and trifluoroacetic acid

Baskaran, Subramanian,Hanan, Emily,Byun, Daniel,Shen, Wang

, p. 2107 - 2111 (2004)

2-Aminopyrimidines were facilely reduced to 2-amino-dihydro- or 2-amino-tetrahydropyrimidines with triethylsilane and trifluroacetic acid in high yields. By controlling the equivalents of reducing reagents and temperature, selective reduction could also be achieved for some substrates.

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