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13219-76-6

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13219-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13219-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,1 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13219-76:
(7*1)+(6*3)+(5*2)+(4*1)+(3*9)+(2*7)+(1*6)=86
86 % 10 = 6
So 13219-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4/c1-6-8(4-5-9(13)16-3)7(2)12-10(6)11(14)15/h12H,4-5H2,1-3H3,(H,14,15)

13219-76-6SDS

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 4-(3-methoxy-3-oxopropyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-3-propanoicacid,5-carboxy-2,4-dimethyl-,3-methyl ester

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:13219-76-6 SDS

13219-76-6Relevant articles and documents

Investigations regarding the utility of prodigiosenes to treat leukemia

Smithen, Deborah A.,Forrester, A. Michael,Corkery, Dale P.,Dellaire, Graham,Colpitts, Julie,McFarland, Sherri A.,Berman, Jason N.,Thompson, Alison

, p. 62 - 68 (2013/02/23)

Prodigiosenes, possessing a 4-methoxypyrrolyldipyrrin skeleton, are known for their anti-cancer activity. Structural modification of the C-ring resulted in a series of prodigiosenes that displayed promising activity against leukemia cell lines during in v

Novel inhibitor for fibroblast growth factor receptor tyrosine kinase

Kammasud, Naparat,Boonyarat, Chantana,Tsunoda, Satoshi,Sakurai, Hiroaki,Saiki, Ikuo,Grierson, David S.,Vajragupta, Opa

, p. 4812 - 4818 (2008/02/12)

NP603, the 6-dimethoxy phenyl indolin-2-one, was designed as FGF receptor 1 inhibitor by computational study. NP603 was synthesized and found to be more active against endothelial proliferation of HUVEC after the rhFGF-2 stimulation than SU6668 with minim

Indolinone compounds as kinase inhibitors

-

Page/Page column 96, (2010/11/30)

The invention relates to certain indolinone compounds, their method of synthesis, and a combinatorial library consisting of the indolinone compounds of the invention. The invention also relates to methods of modulating the function of protein kinases using indolinone compounds of the invention and methods of treating diseases by modulating the function of protein kinases and related signal transduction pathways.

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