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109448-23-9

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109448-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109448-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,4 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109448-23:
(8*1)+(7*0)+(6*9)+(5*4)+(4*4)+(3*8)+(2*2)+(1*3)=129
129 % 10 = 9
So 109448-23-9 is a valid CAS Registry Number.

109448-23-9SDS

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 3-(4-methylphenyl)sulfanyl-1-phenylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-p-Tolylmercapto-N-phenyl-succinimid

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:109448-23-9 SDS

109448-23-9Relevant articles and documents

Iodine-Promoted C(sp 2)-H thiolation of maleimides with dimethyl sulfoxide and thiols

Tan, Hong-Ru,Wang, Lun,Yang, Zhen-Hua,Zhao, Sheng-Yin,Zhu, Jia-Nan

, p. 4113 - 4123 (2018/10/15)

Iodine-promoted C(sp 2)-H methylthiolation of maleimides using DMSO as synthon has been developed to afford 3-methylthiomaleimides in moderate yields under metal-free conditions. In addition, 3-thiomaleimides were synthesized from maleimides an

Copper-catalyzed intermolecular thioamination of maleimides with thiols and formamides: A one-step construction of 3-Amino-4-Thiomaleimides using formamides as nitrogen sources

Yang, Zhen-Hua,Zhu, Jia-Nan,Jin, Ze-Hui,Zheng, Jian,Zhao, Sheng-Yin

, p. 4627 - 4636 (2019/02/01)

A highly efficient copper-catalyzed intermolecular C(sp2)-H thioamination of maleimides with thiols and formamides in the presence of fluoroboric acid is reported using various readily available formamides as nitrogen sources and solvents. A diverse range of 3-Amino-4-Thiomaleimides is obtained with good yields under mild conditions, involving C-N and C-S bond formation. This methodology enriches current C-N and C-S bond formation chemistry and features operational simplicity and excellent functional-group tolerance.

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