Cas 1073796-65-2,5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate

1073796-65-2

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Basic information

Product Name: 5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate
Synonyms: 5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate
CAS NO:1073796-65-2
Molecular Formula:
Molecular Weight: 546.313
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: 5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate(CAS DataBase Reference)
NIST Chemistry Reference: 5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate(1073796-65-2)
EPA Substance Registry System: 5-acetoxymethyl-2,3-dimethoxyphenyl 2-iodo-3,4,5-trimethoxybenzoate(1073796-65-2)

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: 1073796-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1073796-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,7,9 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1073796-65:
(9*1)+(8*0)+(7*7)+(6*3)+(5*7)+(4*9)+(3*6)+(2*6)+(1*5)=182
182 % 10 = 2
So 1073796-65-2 is a valid CAS Registry Number.

1073796-65-2Upstream product

98799-41-8 2-iodo-3,4,5-trimethoxybenzoic acid

1073796-65-2Downstream Products

1073796-65-2Relevant academic research and scientific papers

Synthesis of highly oxygenated biphenyl derivative in an optically active form through palladium-mediated intramolecular biaryl coupling reaction

Abe, Hitoshi,Arai, Masatsugu,Nishioka, Keisuke,Kida, Tatsuya,Shioe, Kazuma,Takeuchi, Yasuo,Harayama, Takashi

, p. 291 - 303 (2008)

Optically active 6,6'-dihydroxymethyl-2,2'-3,3'-4,4'-hexamethoxybiphenyl (1) was prepared via the Pd-mediated biaryl coupling reaction of a phenyl benzoate derivative and the following enantioselective lactone opening reaction. The Japan Institute of Hete

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