Cas 1125824-25-0,ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate

1125824-25-0

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Basic information

Product Name: ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate
Synonyms: ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate
CAS NO:1125824-25-0
Molecular Formula:
Molecular Weight: 305.334
EINECS: N/A
Product Categories: N/A
Mol File: 1125824-25-0.mol
Article Data: 2

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: ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate(1125824-25-0)
EPA Substance Registry System: ethyl-3-(5-azido-2-phenyl-1,3-dioxan-4-yl)propanoate(1125824-25-0)

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: 1125824-25-0(Hazardous Substances Data)

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1125824-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1125824-25-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,5,8,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1125824-25:
(9*1)+(8*1)+(7*2)+(6*5)+(5*8)+(4*2)+(3*4)+(2*2)+(1*5)=130
130 % 10 = 0
So 1125824-25-0 is a valid CAS Registry Number.

1125824-25-0Upstream product

1125824-25-0Downstream Products

1125824-76-1 2-phenyltetrahydro-4H-(1,3)dioxino(5,4-b)pyridin-6(7H)-one

1125824-25-0Relevant articles and documents

A regioselective reductive cleavage of benzylidene acetal: stereoselective synthesis of N-Boc-protected cis-(2R,3S)-3-hydroxy pipecolic acid

Kumar, Ponminor Senthil,Baskaran, Sundarababu

, p. 3489 - 3492 (2009)

A stereoselective synthesis of N-Boc-protected cis-(2R,3S)-3-hydroxy pipecolic acid, starting from d-glucose is described. The key step in the overall synthesis is a highly regioselective reductive cleavage of benzylidene acetal 13 leading to hydroxymethy

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