Cas 1309750-33-1,(E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate

1309750-33-1

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Basic information

Product Name: (E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate
Synonyms: (E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate
CAS NO:1309750-33-1
Molecular Formula:
Molecular Weight: 424.61
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: (E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate(1309750-33-1)
EPA Substance Registry System: (E)-methyl 4-(tert-butyldimethylsilyloxy)-3-(3-(4-methoxybenzyloxy)propoxy)but-2-enoate(1309750-33-1)

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: 1309750-33-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309750-33-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,7,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1309750-33:
(9*1)+(8*3)+(7*0)+(6*9)+(5*7)+(4*5)+(3*0)+(2*3)+(1*3)=151
151 % 10 = 1
So 1309750-33-1 is a valid CAS Registry Number.

1309750-33-1Upstream product

1309750-33-1Downstream Products

1309750-33-1Relevant academic research and scientific papers

Synthetic and computational studies of acyl radical cyclizations with β-alkoxyacrylates: Formal synthesis of (±)-longianone

Aitken, Heather M.,Schiesser, Carl H.,Donner, Christopher D.

, p. 409 - 415 (2011)

An investigation into the cyclization of acyl radicals with mono- and disubstituted β-alkoxyacrylates is described. Ether-tethered acyl radicals, generated directly from the corresponding aldehyde, undergo cyclization to form dioxaspiro heterocyclic syste

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