Cas 1332726-65-4,tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate

1332726-65-4

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Basic information

Product Name: tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate
Synonyms: tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate
CAS NO:1332726-65-4
Molecular Formula:
Molecular Weight: 500.596
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: tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate(1332726-65-4)
EPA Substance Registry System: tert-butyl (S)-1-[4-(diethoxyphosphoryl)-tetrahydro-2H-thiopyran-4-ylamino]-1-oxo-3-phenylpropan-2-carbamate(1332726-65-4)

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: 1332726-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332726-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,7,2 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1332726-65:
(9*1)+(8*3)+(7*3)+(6*2)+(5*7)+(4*2)+(3*6)+(2*6)+(1*5)=144
144 % 10 = 4
So 1332726-65-4 is a valid CAS Registry Number.

1332726-65-4Upstream product

13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine

1332726-65-4Downstream Products

1332726-65-4Relevant academic research and scientific papers

Synthesis of an enkephalin analogue containing an α,α- disubstituted heterocyclic aminophosphonic acid

Rabasso, Nicolas,Fadel, Antoine

, p. 1811 - 1819 (2011)

Synthesis of a phosphonopentapeptide enkephalin analogue was achieved from heterocyclic aminophosphonates via the coupling of Boc-Tyr-Gly-Gly-OH with phosphonodipeptide. The latter was formed by coupling Boc-Phe-OH with N-terminal α,α-disubstituted hetero

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