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190273-74-6

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190273-74-6 Usage

Chemical compound

2-Amino-5-(trifluoromethyl)quinazoline

Classification

Quinazoline

Appearance

White solid

Pharmaceutical interest

Potential anti-cancer agent

Mechanism of action

Inhibition of enzymes involved in cancer cell proliferation

Applications

Synthesis of organic compounds, reagent in chemical reactions

Scientific interest

Subject of investigation in medicinal chemistry and organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 190273-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,2,7 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190273-74:
(8*1)+(7*9)+(6*0)+(5*2)+(4*7)+(3*3)+(2*7)+(1*4)=136
136 % 10 = 6
So 190273-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F3N3/c10-9(11,12)6-2-1-3-7-5(6)4-14-8(13)15-7/h1-4H,(H2,13,14,15)

190273-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(trifluoromethyl)quinazolin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-5-(trifluoromethyl)quinazoline

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:190273-74-6 SDS

190273-74-6Downstream Products

190273-74-6Relevant articles and documents

Synthesis of 2-Aminoquinazolines from ortho-Fluorobenzaldehydes

Hynes, John B.,Campbell, Johnny P.

, p. 385 - 387 (2007/10/03)

The reaction of guanidine carbonate with various ortho-fluorobenzaldehydes in N,N-dimethylacetamide was investigated as a potential route for preparing 2-aminoquinazolines. Eleven new 2-aminoquinazolines were elaborated in this manner in low to moderate yields. In general the best results were obtained with ortho-fluorobenzaldehydes possessing an electron withdrawing substituent at the other ortho position. Complex mixtures were obtained using 2-fluorobenzaldehyde, 2,5-difluorobenzaldehyde and 2-fluoro-5-methoxybenzaldehyde which were not resolved.

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