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128256-22-4

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128256-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128256-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,5 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128256-22:
(8*1)+(7*2)+(6*8)+(5*2)+(4*5)+(3*6)+(2*2)+(1*2)=124
124 % 10 = 4
So 128256-22-4 is a valid CAS Registry Number.

128256-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2,4-diphenyl-1,4-dihydroquinazoline

1.2 Other means of identification

Product number -
Other names Quinazoline,1,4-dihydro-6-methyl-2,4-diphenyl

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:128256-22-4 SDS

128256-22-4Downstream Products

128256-22-4Relevant articles and documents

Cycloaddition reactions of 2,4-diphenyl-1,3-diazabuta-1,3-dienes with isocyanates and isothiocyanates

Abbiati, Giorgio,De Carvalho, Alessandro Cirrincione,Rossi, Elisabetta

, p. 7397 - 7402 (2007/10/03)

The cycloaddition reactions of 1-p-tolyl and 1-benzyl- 2,4-diphenyl-1,3-diazabuta-1,3-dienes with a variety of aryl and alkyl isocyanate and isothiocyanate are described. The reaction mechanism is also discussed.

A convenient synthesis of Quinazoline ring by tandem aza-Wittig reaction/electrocyclic ring closure

Rossi,Calabrese,Farma

, p. 5819 - 5834 (2007/10/02)

3,4-D-Dihydroquinazolines and Quinazolines were prepared starting from N'-aryl-N-(triphenylphosphoranilidene)-carboximidamides and aliphatic or aromatic aldehydes. The mechanism of the reaction is discussed.

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