Cas 220185-67-1,(2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester

220185-67-1

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Basic information

Product Name: (2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester
Synonyms: (2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester
CAS NO:220185-67-1
Molecular Formula:
Molecular Weight: 326.179
EINECS: N/A
Product Categories: N/A

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: (2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester(220185-67-1)
EPA Substance Registry System: (2Z,4E)-7-(2-Amino-4,5-dichloro-phenyl)-2-methoxy-hepta-2,4-dien-6-ynoic acid methyl ester(220185-67-1)

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: 220185-67-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220185-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 220185-67:
(8*2)+(7*2)+(6*0)+(5*1)+(4*8)+(3*5)+(2*6)+(1*7)=101
101 % 10 = 1
So 220185-67-1 is a valid CAS Registry Number.

220185-67-1Upstream product

220185-67-1Downstream Products

220185-67-1Relevant academic research and scientific papers

Synthesis of 2-dienylindole, SB 242784, by a three-component palladium- catalyzed coupling reaction

Yu, Marvin S.,Lopez De Leon, Lewilynn,McGuire, Michael A.,Botha, Glen

, p. 9347 - 9350 (1998)

The synthesis of SB 242784 using a novel one-pot Castro-Stephens-Suzuki reaction as the key reaction is described.

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