Cas 114475-42-2,(E)-2-Benzyl-3-((2R,3S)-3-tert-butoxycarbonylamino-5-oxo-tetrahydro-furan-2-yl)-acrylic acid benzyl ester

114475-42-2

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Basic information

Product Name: (E)-2-Benzyl-3-((2R,3S)-3-tert-butoxycarbonylamino-5-oxo-tetrahydro-furan-2-yl)-acrylic acid benzyl ester
Synonyms:
CAS NO:114475-42-2
Molecular Formula:
Molecular Weight: 451.519
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: (E)-2-Benzyl-3-((2R,3S)-3-tert-butoxycarbonylamino-5-oxo-tetrahydro-furan-2-yl)-acrylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-Benzyl-3-((2R,3S)-3-tert-butoxycarbonylamino-5-oxo-tetrahydro-furan-2-yl)-acrylic acid benzyl ester(114475-42-2)
EPA Substance Registry System: (E)-2-Benzyl-3-((2R,3S)-3-tert-butoxycarbonylamino-5-oxo-tetrahydro-furan-2-yl)-acrylic acid benzyl ester(114475-42-2)

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: 114475-42-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114475-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,7 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114475-42:
(8*1)+(7*1)+(6*4)+(5*4)+(4*7)+(3*5)+(2*4)+(1*2)=112
112 % 10 = 2
So 114475-42-2 is a valid CAS Registry Number.

114475-42-2Upstream product

114475-33-1 (E)-(S)-4-Acetoxy-2-benzyl-5-tert-butoxycarbonylamino-hept-2-enedioic acid 1-benzyl ester 7-tert-butyl ester

114475-42-2Downstream Products

114475-42-2Relevant academic research and scientific papers

AMIDE BOND SURROGATES: A GENERAL SYNTHETIC ROUTE TO TRANS CARBON-CARBON DOUBLE BOND ISOSTERES.

Shue, Youe-Kong,Carrera, George M.,Nadzan, Jr.,Nadzan, Alex M.

, p. 3225 - 3228 (1987)

A practical synthesis toward trans double bond replacements of amide bond pseudopeptides has been accomplished.This methodology provides a general route to a wide range of modified peptide analogs which may have biological significance.

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