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7-amino-3-(2-bromoethoxy)-4-chloroisocoumarin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126062-22-4

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126062-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126062-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126062-22:
(8*1)+(7*2)+(6*6)+(5*0)+(4*6)+(3*2)+(2*2)+(1*2)=94
94 % 10 = 4
So 126062-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrClNO3/c12-3-4-16-11-9(13)7-2-1-6(14)5-8(7)10(15)17-11/h1-2,5H,3-4,14H2

126062-22-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-amino-3-(2-bromoethoxy)-4-chloroisochromen-1-one

1.2 Other means of identification

Product number -
Other names 7-amino-3-(2-bromoethoxy)-4-chloroisocoumarin

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:126062-22-4 SDS

126062-22-4Relevant academic research and scientific papers

Alkyne derivatives of isocoumarins as clickable activity-based probes for serine proteases

Haedke, Ute,G?tz, Markus,Baer, Philipp,Verhelst, Steven H.L.

, p. 633 - 640 (2012/03/11)

Activity-based probes (ABPs) have found increasing use in functional proteomics studies. Recently, ABPs that can be employed in combination with click chemistry gained particular attention due to their flexible application in vitro and in vivo. Moreover,

Isocoumarin-based inhibitors of urokinase-type plasminogen activator

-

Page/Page column 6, (2008/06/13)

The present invention relates to chemical compounds, pharmaceutical compositions and methods for treating tumors and cancer and diseases which involve angiogenesis including retinopathy, age-related macular degeneration, angiogenic skin disorders and infl

Synthesis of new 3-alkoxy-7-amino-4-chloro-isocoumarin derivatives as new β-amyloid peptide production inhibitors and their activities on various classes of protease

Bihel, Frederic,Quelever, Gilles,Lelouard, Hugues,Petit, Agnes,Da Costa, Cristine Alves,Pourquie, Olivier,Checler, Frederic,Thellend, Annie,Pierre, Philippe,Kraus, Jean-Louis

, p. 3141 - 3152 (2007/10/03)

A series of new 7-substituted-4-chloro-3-alkoxy isocoumarin derivatives were synthesized and evaluated as inhibitors of representative classes of proteases: serine protease (α-chymotrypsin, trypsin), cysteine protease (Caspase-3), and aspartyl protease (H

Mechanism-based isocoumarin inhibitors for blood coagulation serine proteases. Effect of the 7-substituent in 7-amino-4-chloro-3- (isothioureidoalkoxy)isocoumarins on inhibitory and anticoagulant potency

Kam,Kerrigan,Plaskon,Duffy,Lollar,Suddath,Powers

, p. 1298 - 1306 (2007/10/02)

A series of 7-amino-4-chloro-3-(3-isothioureidopropoxy)isocoumarin (NH2- CiTPrOIC) derivatives with various substituents at the 7- and 3-positions have been synthesized as inhibitors of several blood coagulation enzymes. Isocoumarins substitute

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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