Cas 1229574-01-9,t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate

1229574-01-9

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Basic information

Product Name: t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate
Synonyms: t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate
CAS NO:1229574-01-9
Molecular Formula:
Molecular Weight: 597.827
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: t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate(CAS DataBase Reference)
NIST Chemistry Reference: t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate(1229574-01-9)
EPA Substance Registry System: t-butyl 4-{7-[(t-butyldimethylsilyl)oxy]-2-oxo-2H-chromen-4-yl}-[2-diphenyl(methylidene)amino]butanoate(1229574-01-9)

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: 1229574-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1229574-01-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,5,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1229574-01:
(9*1)+(8*2)+(7*2)+(6*9)+(5*5)+(4*7)+(3*4)+(2*0)+(1*1)=159
159 % 10 = 9
So 1229574-01-9 is a valid CAS Registry Number.

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1229574-01-9Relevant academic research and scientific papers

Synthesis of the fluorescent amino acid rac-(7-hydroxycoumarin-4-yl) ethylglycine

Braun, Manfred,Dittrich, Torsten

, (2010)

The hydrochloride of the racemic amino acid (7-hydroxycoumarin-4-yl) ethylglycine, a versatile fluorescent probe in proteins, has been synthesized in five steps from commercially available (7-hydroxycoumarin-4-yl)acetic acid. The key step involves the alkylation of a glycine-enolate equivalent.

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