Cas 202145-92-4,{4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester

202145-92-4

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Basic information

Product Name: {4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester
Synonyms: {4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester
CAS NO:202145-92-4
Molecular Formula:
Molecular Weight: 650.857
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: {4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester(202145-92-4)
EPA Substance Registry System: {4-[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-{3-[3-(4-hydroxy-phenyl)-propionylamino]-propyl}-carbamic acid tert-butyl ester(202145-92-4)

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: 202145-92-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 202145-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,4 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 202145-92:
(8*2)+(7*0)+(6*2)+(5*1)+(4*4)+(3*5)+(2*9)+(1*2)=84
84 % 10 = 4
So 202145-92-4 is a valid CAS Registry Number.

202145-92-4Upstream product

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202145-92-4Relevant academic research and scientific papers

Practical synthesis of unsymmetrical polyamine amides

Blagbrough, Ian S.,Geall, Andrew J.

, p. 439 - 442 (2007/10/03)

Desymmetrisation of readily available symmetrical polyamines is an important first step in the synthesis of many polyamine containing natural products. Likewise in the synthesis of polyamine amides which are potentially useful for gene delivery and as neuroprotectants, based upon channel blocking toxins found in certain wasp and spider venoms. The application of trifluoroacetyl as a protecting group allows unsymmetrical polyamine amides to be easily prepared on a gram scale.

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