Cas 74741-37-0,(2S,3S)-2-(3,4-Dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester

74741-37-0

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Basic information

Product Name: (2S,3S)-2-(3,4-Dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester
Synonyms:
CAS NO:74741-37-0
Molecular Formula:
Molecular Weight: 374.39
EINECS: N/A
Product Categories: N/A
Mol File: 74741-37-0.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: (2S,3S)-2-(3,4-Dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-2-(3,4-Dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester(74741-37-0)
EPA Substance Registry System: (2S,3S)-2-(3,4-Dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester(74741-37-0)

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: 74741-37-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74741-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74741-37:
(7*7)+(6*4)+(5*7)+(4*4)+(3*1)+(2*3)+(1*7)=140
140 % 10 = 0
So 74741-37-0 is a valid CAS Registry Number.

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74741-37-0Relevant articles and documents

Benzodioxans by Oxidative Phenol Coupling. Synthesis of Silybin

Merlini, Lucio,Zanarotti, Antonio,Pelter, Andrew,Rochefort, Malcolm P.,Haensel, Rudolf

, p. 775 - 778 (2007/10/02)

Oxidative coupling of substituted catechols with isoeugenol or coniferyl alcohol in the presence of silver oxide affords 2,3-trans-1,4-benzodioxans in good yield.The reaction is highly regioselective when the catechol bears an alkyl substituent, much less

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