Cas 1446270-28-5,(S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate

1446270-28-5

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Basic information

Product Name: (S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate
Synonyms: (S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate
CAS NO:1446270-28-5
Molecular Formula:
Molecular Weight: 338.452
EINECS: N/A
Product Categories: N/A
Mol File: 1446270-28-5.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate(1446270-28-5)
EPA Substance Registry System: (S)-2-((2, 3-dimethylphenyl)amino)-2-oxoethyl(2-oxotetrahydrofuran-3-yl)carbamodithioate(1446270-28-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1446270-28-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1446270-28-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,2,7 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1446270-28:
(9*1)+(8*4)+(7*4)+(6*6)+(5*2)+(4*7)+(3*0)+(2*2)+(1*8)=155
155 % 10 = 5
So 1446270-28-5 is a valid CAS Registry Number.

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1446270-28-5Relevant articles and documents

Design, synthesis and antibacterial evaluation of novel AHL analogues

Ren, Jing-Li,Zhang, En,Ye, Xian-Wei,Wang, Meng-Meng,Yu, Bin,Wang, Wen-Hua,Guo, Ya-Zhuo,Liu, Hong-Min

, p. 4154 - 4156 (2013)

Two series of novel AHL analogues were designed, synthesized and evaluated for antibacterial activity under cell membrane conditions in vitro. Analogues 4a-c and 4g-m presented potent activity against Gram-positive bacteria. Especially the analogue 4l exe

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