Cas 244262-53-1,[(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane

244262-53-1

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Basic information

Product Name: [(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane
Synonyms: [(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane
CAS NO:244262-53-1
Molecular Formula:
Molecular Weight: 405.093
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: [(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane(244262-53-1)
EPA Substance Registry System: [(Z)-1-Chloromethyl-3-methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enyloxy]-triisopropyl-silane(244262-53-1)

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: 244262-53-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 244262-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,6 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 244262-53:
(8*2)+(7*4)+(6*4)+(5*2)+(4*6)+(3*2)+(2*5)+(1*3)=121
121 % 10 = 1
So 244262-53-1 is a valid CAS Registry Number.

244262-53-1Upstream product

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244262-53-1Relevant academic research and scientific papers

Macrocyclic studies of EZ and ZZ 12-membered aza macrocycles; Novel molecular rearrangement observed

Bourque, élyse,Grenon, Michel,Laliberté, Sébastien,Deslongchamps, Pierre

, p. 1115 - 1117 (1999)

EZ and ZZ hetero macrocyclic dienes 13a and 14b are generated respectively by an intramolecular displacement of α-chloroketones 11a and 11b using trifluoroacetamide as nucleophilic agent. Novel molecular rearrangements were observed.

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