Cas 147227-80-3,4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate

147227-80-3

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Basic information

Product Name: 4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate
Synonyms: 4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate
CAS NO:147227-80-3
Molecular Formula:
Molecular Weight: 470.481
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: 4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate(CAS DataBase Reference)
NIST Chemistry Reference: 4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate(147227-80-3)
EPA Substance Registry System: 4-((9-fluorenylmethoxy)carboxamido)phenylacetic acid N-hydroxysuccinimidate(147227-80-3)

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: 147227-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147227-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,2 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147227-80:
(8*1)+(7*4)+(6*7)+(5*2)+(4*2)+(3*7)+(2*8)+(1*0)=133
133 % 10 = 3
So 147227-80-3 is a valid CAS Registry Number.

147227-80-3Upstream product

74124-79-1 di(succinimido) carbonate

147227-80-3Downstream Products

147227-80-3Relevant academic research and scientific papers

Prodrugs of Doxorubicin and Melphalan and Their Activation by a Monoclonal Antibody-Penicillin-G Amidase Conjugate

Vrudhula, Vivekananda M.,Senter, Peter D.,Fischer, Keith J.,Wallace, Philip M.

, p. 919 - 923 (1993)

The syntheses and cytotoxic activities of substituted N-phenylacetamido derivatives of doxorubicin and melphalan are described.The derivatives were designed as prodrugs which could be activated in a site-specific manner by monoclonal antibody-penicillin-G

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