Cas 141468-60-2,Carbamic acid, [2-[[3-(2-bromoethoxy)-4-chloro-1-oxo-1H-2-benzopyran-7-yl]amino]-2- oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (R)-

141468-60-2

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Basic information

Product Name: Carbamic acid, [2-[[3-(2-bromoethoxy)-4-chloro-1-oxo-1H-2-benzopyran-7-yl]amino]-2- oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (R)-
Synonyms:
CAS NO:141468-60-2
Molecular Formula: C25H26BrClN2O6
Molecular Weight: 565.848
EINECS: N/A
Product Categories: N/A
Mol File: 141468-60-2.mol

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: Carbamic acid, [2-[[3-(2-bromoethoxy)-4-chloro-1-oxo-1H-2-benzopyran-7-yl]amino]-2- oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (R)-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-[[3-(2-bromoethoxy)-4-chloro-1-oxo-1H-2-benzopyran-7-yl]amino]-2- oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (R)-(141468-60-2)
EPA Substance Registry System: Carbamic acid, [2-[[3-(2-bromoethoxy)-4-chloro-1-oxo-1H-2-benzopyran-7-yl]amino]-2- oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (R)-(141468-60-2)

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: 141468-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141468-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141468-60:
(8*1)+(7*4)+(6*1)+(5*4)+(4*6)+(3*8)+(2*6)+(1*0)=122
122 % 10 = 2
So 141468-60-2 is a valid CAS Registry Number.

141468-60-2Upstream product

141468-60-2Downstream Products

141468-60-2Relevant academic research and scientific papers

Mechanism-Based Isocoumarin Inhibitors for Human Leukocyte Elastase. Effect of the 7-Amino Substituent and 3-Alkoxy Group in 3-Alkoxy-7-amino-4-chloroisocoumarins on Inhibitory Potency

Kerrigan, John E.,Oleksyszyn, Jozef,Kam, Chih-Min,Selzler, Joe,Powers, James C.

, p. 544 - 552 (2007/10/02)

A series of 3-alkoxy-7-amino-4-chloroisocoumarins with various 3-alkoxy substituents have been prepared and evaluated as inhibitors of human leukocyte elastase (HLE).In addition, a new series of acyl, urea, and carbamate derivatives of 7-amino-4-chloro-3-

SUBSTITUTED ISOCOUMARINS

-

, (2008/06/13)

Substituted isocoumarins, their use in inhibiting serine proteases with chymotrypsin-like and elastase-like specificity and their roles as anti-inflammatory agents.

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