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61741-42-2

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61741-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61741-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,4 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61741-42:
(7*6)+(6*1)+(5*7)+(4*4)+(3*1)+(2*4)+(1*2)=112
112 % 10 = 2
So 61741-42-2 is a valid CAS Registry Number.

61741-42-2SDS

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-[(4-methoxyphenyl)methylamino]-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-(4-methoxy-benzylamino)-3H-quinazolin-4-one

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:61741-42-2 SDS

61741-42-2Downstream Products

61741-42-2Relevant articles and documents

The method of synthesis of quinazolinone derivative

-

Paragraph 0026; 0027; 0028; 0029; 0030, (2019/03/26)

The invention discloses a method for synthesizing quinazolinone derivatives, from the commercialization or easy synthesis of 2 - amino quinazolinone starting, by carrying out the alkylation reaction of the alcohol, the obtained quinazolinone derivatives.

Odorless isocyanide chemistry: An integrated microfluidic system for a multistep reaction sequence

Sharma, Siddharth,Maurya, Ram Awatar,Min, Kyoung-Ik,Jeong, Guan-Young,Kim, Dong-Pyo

supporting information, p. 7564 - 7568 (2013/07/26)

Can't smell this: An integrated continuous-flow microfluidic setup enables in situ generation, extraction, separation, and reaction of foul-smelling isocyanides with little exposure to the surroundings. Isocyanides were generated by dehydration of the corresponding N-substituted formamides, and several representative isocyanide-based organic reactions were successfully performed. DIPEA=N,N-diisopropylethylamine. Copyright

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