Cas 1190409-13-2,chloro-acetic acid 3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl ester

1190409-13-2

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Basic information

Product Name: chloro-acetic acid 3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl ester
Synonyms:
CAS NO:1190409-13-2
Molecular Formula:
Molecular Weight: 707.564
EINECS: N/A
Product Categories: N/A
Mol File: 1190409-13-2.mol
Article Data: 1

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: chloro-acetic acid 3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: chloro-acetic acid 3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl ester(1190409-13-2)
EPA Substance Registry System: chloro-acetic acid 3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl ester(1190409-13-2)

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: 1190409-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190409-13-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,4,0 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1190409-13:
(9*1)+(8*1)+(7*9)+(6*0)+(5*4)+(4*0)+(3*9)+(2*1)+(1*3)=132
132 % 10 = 2
So 1190409-13-2 is a valid CAS Registry Number.

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1190409-13-2Relevant articles and documents

Novel hybrid natural products derived from solanesol as wound healing agents

Srivastava, Shefali,Raj, Kanwal,Khare, Pratibha,Bhaduri, Amiya P.,Chander, Ramesh,Raghubir, Ram,Mahendra,Rao,Prabhu

experimental part, p. 237 - 247 (2009/12/09)

A series of compounds 2a-g, 3a,b, 4a-n have been synthesized from solanesol 1, an acyclic terpenoid alcohol, extracted from tobacco waste. These compounds have been evaluated for antioxidant, angiogenesis and wound healing activity. Compounds 3b and 4h ex

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