Cas 404373-05-3,2-Naphthalenol, 1,2,3,4-tetrahydro-5,8-dimethoxy-3-[(4-methoxyphenyl)amino]-, (2R,3R)-

404373-05-3

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Basic information

Product Name: 2-Naphthalenol, 1,2,3,4-tetrahydro-5,8-dimethoxy-3-[(4-methoxyphenyl)amino]-, (2R,3R)-
Synonyms:
CAS NO:404373-05-3
Molecular Formula: C19H23NO4
Molecular Weight: 329.396
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: 2-Naphthalenol, 1,2,3,4-tetrahydro-5,8-dimethoxy-3-[(4-methoxyphenyl)amino]-, (2R,3R)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Naphthalenol, 1,2,3,4-tetrahydro-5,8-dimethoxy-3-[(4-methoxyphenyl)amino]-, (2R,3R)-(404373-05-3)
EPA Substance Registry System: 2-Naphthalenol, 1,2,3,4-tetrahydro-5,8-dimethoxy-3-[(4-methoxyphenyl)amino]-, (2R,3R)-(404373-05-3)

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: 404373-05-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 404373-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,7 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 404373-05:
(8*4)+(7*0)+(6*4)+(5*3)+(4*7)+(3*3)+(2*0)+(1*5)=113
113 % 10 = 3
So 404373-05-3 is a valid CAS Registry Number.

404373-05-3Upstream product

104-94-9 4-methoxy-aniline

404373-05-3Downstream Products

404373-05-3Relevant academic research and scientific papers

An enantioselective formal synthesis of 4-demethoxydaunomycin using the catalytic asymmetric ring opening reaction of meso-epoxide with p-anisidine

Sekine, Akihiro,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 75 - 82 (2002)

A catalytic asymmetric formal synthesis of 4-demethoxydaunomycin (3) was achieved using a catalytic asymmetric ring opening reaction of meso-epoxide 9 as a key step. The epoxide opening reaction was promoted by 10 mol% of Pr-(R)-BINOL-Ph3P=O co

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