Cas 138395-84-3,(S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (2R,3S,5R)-5-[6-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester

138395-84-3

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Basic information

Product Name: (S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (2R,3S,5R)-5-[6-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester
Synonyms:
CAS NO:138395-84-3
Molecular Formula:
Molecular Weight: 745.833
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-tert-Butoxycarbonylamino-3-phenyl-propionic acid (2R,3S,5R)-5-[6-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (2R,3S,5R)-5-[6-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(138395-84-3)
EPA Substance Registry System: (S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (2R,3S,5R)-5-[6-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(138395-84-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 138395-84-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138395-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138395-84:
(8*1)+(7*3)+(6*8)+(5*3)+(4*9)+(3*5)+(2*8)+(1*4)=163
163 % 10 = 3
So 138395-84-3 is a valid CAS Registry Number.

138395-84-3Upstream product

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138395-84-3Relevant academic research and scientific papers

AMINOACYLATION OF NUCLEOSIDES. MITSUNOBU CONDITIONS versus CHEMOENZYMATIC ROUTE

Montero, J-L.,Criton, M.,Dewynter, G-F.,Imbach, J-L.

, p. 5357 - 5358 (1991)

Aminoacylation of thymidine and deoxyadenosine by phenylalanine was carried out using the PPh3-DEAD reagent or subtilisin. Key Words: aminoacylation, nucleosides, Mitsunobu reaction, subtilisin.

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