Cas 1030600-36-2,benzyl 4-[{2-[2-(benzyloxycarbonylamino)-3-phenylpropionyloxy]-3-isopropoxy-4-methoxybenzyl}(tert-butoxycarbonyl)amino]butyrate

1030600-36-2

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Basic information

Product Name: benzyl 4-[{2-[2-(benzyloxycarbonylamino)-3-phenylpropionyloxy]-3-isopropoxy-4-methoxybenzyl}(tert-butoxycarbonyl)amino]butyrate
Synonyms:
CAS NO:1030600-36-2
Molecular Formula:
Molecular Weight: 768.904
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 4-[{2-[2-(benzyloxycarbonylamino)-3-phenylpropionyloxy]-3-isopropoxy-4-methoxybenzyl}(tert-butoxycarbonyl)amino]butyrate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 4-[{2-[2-(benzyloxycarbonylamino)-3-phenylpropionyloxy]-3-isopropoxy-4-methoxybenzyl}(tert-butoxycarbonyl)amino]butyrate(1030600-36-2)
EPA Substance Registry System: benzyl 4-[{2-[2-(benzyloxycarbonylamino)-3-phenylpropionyloxy]-3-isopropoxy-4-methoxybenzyl}(tert-butoxycarbonyl)amino]butyrate(1030600-36-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1030600-36-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1030600-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,6,0 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1030600-36:
(9*1)+(8*0)+(7*3)+(6*0)+(5*6)+(4*0)+(3*0)+(2*3)+(1*6)=72
72 % 10 = 2
So 1030600-36-2 is a valid CAS Registry Number.

1030600-36-2Upstream product

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1030600-36-2Relevant academic research and scientific papers

Improved auxiliary for the synthesis of medium-sized bis(lactams)

Springer, Jasper,Jansen, T. Paul,Ingemann, Steen,Hiemstra, Henk,Van Maarseveen, Jan H.

, p. 361 - 367 (2008/09/18)

Our auxiliary-based method for the synthesis of bis(lactams) has been optimized. A novel auxiliary is described that is inserted in the backbone of a linear peptide facilitating the mutually reactive terminal groups to approach one another for a cyclizati

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