Cas 78043-79-5,(3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester

78043-79-5

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Basic information

Product Name: (3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester
Synonyms: (3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester
CAS NO:78043-79-5
Molecular Formula:
Molecular Weight: 421.496
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: (3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester(78043-79-5)
EPA Substance Registry System: (3-Amino-2,2'-dioxo-4,4'-diphenyl-[1,3']biazetidinyl-1'-yl)-acetic acid tert-butyl ester(78043-79-5)

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: 78043-79-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78043-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78043-79:
(7*7)+(6*8)+(5*0)+(4*4)+(3*3)+(2*7)+(1*9)=145
145 % 10 = 5
So 78043-79-5 is a valid CAS Registry Number.

78043-79-5Upstream product

78043-79-5Downstream Products

78029-10-4 Ac-(L/D)Phe-(D/L)Phe-Gly-OtBu

78043-79-5Relevant academic research and scientific papers

β-LACTAM AS SYNTHETIC INTERMEDIATE. A NEW SYNTHETIC APPROACH TO OLIGOPEPTIDES THROUGH NOVEL β-LACTAMS

Hatanaka, Naoto,Ojima, Iwao

, p. 231 - 234 (2007/10/02)

Synthetic method of a new class of β-lactams, which have two b-lactams in a single molecule, was established and subsequent cleavage upon hydrogenolysis by the use of palladium catalyst gave tri- or tetrapeptides, thus providing a new approach to oligopep

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