Cas 233675-63-3,2-Butenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, phenylmethyl ester, (2Z)-

233675-63-3

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Basic information

Product Name: 2-Butenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, phenylmethyl ester, (2Z)-
Synonyms:
CAS NO:233675-63-3
Molecular Formula: C26H23NO4
Molecular Weight: 413.473
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-Butenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, phenylmethyl ester, (2Z)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Butenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, phenylmethyl ester, (2Z)-(233675-63-3)
EPA Substance Registry System: 2-Butenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, phenylmethyl ester, (2Z)-(233675-63-3)

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: 233675-63-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 233675-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,6,7 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 233675-63:
(8*2)+(7*3)+(6*3)+(5*6)+(4*7)+(3*5)+(2*6)+(1*3)=143
143 % 10 = 3
So 233675-63-3 is a valid CAS Registry Number.

233675-63-3Upstream product

73724-48-8 N-(fluoren-9-ylmethoxycarbonyl)-L-threonine benzyl ester

233675-63-3Downstream Products

174879-28-8 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid

233675-63-3Relevant academic research and scientific papers

Dehydration of threonine esters during tosylation

Somlai,Lovas,Forgo,Murphy,Penke

, p. 3633 - 3640 (2001)

Tosylation of N-α-protected threonine methyl-and benzyl esters was investigated. Depending on the protecting groups, the composition of the reaction mixtures showed different ratio between O-tosyl-and dehydrothreonine derivatives. The latter was formed ex

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