Cas 2820-44-2,2-[(1-amino-4-carboxy-1-oxobutan-2-yl)carbamoyl]benzoic acid (non-preferred name)

2820-44-2

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Basic information

Product Name: 2-[(1-amino-4-carboxy-1-oxobutan-2-yl)carbamoyl]benzoic acid (non-preferred name)
Synonyms:
CAS NO:2820-44-2
Molecular Formula: C₁₃H₁₄N₂O₆
Molecular Weight: 294.2601
EINECS: N/A
Product Categories: N/A
Mol File: 2820-44-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 707.8°C at 760 mmHg
Flash Point: 381.9°C
Appearance: N/A
Density: 1.441g/cm³
Vapor Pressure: 4.98E-21mmHg at 25°C
Refractive Index: 1.606
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-[(1-amino-4-carboxy-1-oxobutan-2-yl)carbamoyl]benzoic acid (non-preferred name)(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(1-amino-4-carboxy-1-oxobutan-2-yl)carbamoyl]benzoic acid (non-preferred name)(2820-44-2)
EPA Substance Registry System: 2-[(1-amino-4-carboxy-1-oxobutan-2-yl)carbamoyl]benzoic acid (non-preferred name)(2820-44-2)

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: 2820-44-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2820-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2820-44:
(6*2)+(5*8)+(4*2)+(3*0)+(2*4)+(1*4)=72
72 % 10 = 2
So 2820-44-2 is a valid CAS Registry Number.

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2820-44-2Relevant academic research and scientific papers

Hydrolyzed metabolites of thalidomide: Synthesis and TNF-α production-inhibitory activity

Nakamura, Takanori,Noguchi, Tomomi,Miyachi, Hiroyuki,Hashimoto, Yuichi

, p. 651 - 654 (2008/02/08)

Putative hydrolyzed metabolites of thalidomide were prepared and characterized, and their inhibitory activity on tumor necrosis factor (TNF)-α production in the human monocytic leukemia cell line THP-1 was evaluated. α-(2-Carboxybenzamido)glutarimide was a more potent TNF-α production inhibitor than thalidomide.

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