Cas 127633-34-5,(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionic acid 9,10-dioxo-9,10-dihydro-anthracen-2-ylmethyl ester

127633-34-5

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Basic information

Product Name: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionic acid 9,10-dioxo-9,10-dihydro-anthracen-2-ylmethyl ester
Synonyms:
CAS NO:127633-34-5
Molecular Formula:
Molecular Weight: 623.662
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: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionic acid 9,10-dioxo-9,10-dihydro-anthracen-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionic acid 9,10-dioxo-9,10-dihydro-anthracen-2-ylmethyl ester(127633-34-5)
EPA Substance Registry System: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-phenyl)-propionic acid 9,10-dioxo-9,10-dihydro-anthracen-2-ylmethyl ester(127633-34-5)

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: 127633-34-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127633-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127633-34:
(8*1)+(7*2)+(6*7)+(5*6)+(4*3)+(3*3)+(2*3)+(1*4)=125
125 % 10 = 5
So 127633-34-5 is a valid CAS Registry Number.

127633-34-5Upstream product

127633-34-5Downstream Products

127633-34-5Relevant academic research and scientific papers

Fmoc-polyamide solid phase synthesis of an O-phosphotyrosine-containing tridecapeptide

Kitas,Perich,Wade,Johns,Tregear

, p. 6229 - 6232 (1989)

The incorporation of O-phosphotyrosine into synthetic peptides using Fmoc-Tyr(PO3Me2)-OH in the Fmoc-polyamide procedure is described with the preparation of the model PTyr-tridecapeptide sequence H-Arg-Leu-Ile-Glu-Asp-Asn-Glu-PTyr-T

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