Cas 126166-08-3,benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate

126166-08-3

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Basic information

Product Name: benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate
Synonyms: benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate
CAS NO:126166-08-3
Molecular Formula:
Molecular Weight: 365.429
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: benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate(126166-08-3)
EPA Substance Registry System: benzyl (S)-(1-((2-((tert-butoxycarbonyl)amino)ethyl)amino)-1-oxopropan-2-yl)carbamate(126166-08-3)

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: 126166-08-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126166-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,6 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126166-08:
(8*1)+(7*2)+(6*6)+(5*1)+(4*6)+(3*6)+(2*0)+(1*8)=113
113 % 10 = 3
So 126166-08-3 is a valid CAS Registry Number.

126166-08-3Upstream product

126166-08-3Downstream Products

374756-03-3 N-[2-(2-S-benzyloxycarbonylamino-propanoylamino)ethyl] 2-methanesulfanyl succinamic acid benzyl ester

126166-08-3Relevant academic research and scientific papers

Synthesis and biological evaluation of analogues of the antibiotic pantocin B

Sutton,Clardy

, p. 9935 - 9946 (2001)

Strains of the bacteria Erwinia herbicola produce antibiotics that effectively control E. amylovora, the bacterial pathogen responsible for the plant disease fire blight. Pantocin B was the first of these antibiotics to be characterized, and a flexible sy

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