Cas 1242338-40-4,(2R,3S,6R)-1-benzyloxycarbonyl-3-(tert-butyldimethylsilyloxy)-6-(2-(chloromethyl)allyl)-2-methylpiperidine

1242338-40-4

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Basic information

Product Name: (2R,3S,6R)-1-benzyloxycarbonyl-3-(tert-butyldimethylsilyloxy)-6-(2-(chloromethyl)allyl)-2-methylpiperidine
Synonyms:
CAS NO:1242338-40-4
Molecular Formula:
Molecular Weight: 452.109
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: (2R,3S,6R)-1-benzyloxycarbonyl-3-(tert-butyldimethylsilyloxy)-6-(2-(chloromethyl)allyl)-2-methylpiperidine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,6R)-1-benzyloxycarbonyl-3-(tert-butyldimethylsilyloxy)-6-(2-(chloromethyl)allyl)-2-methylpiperidine(1242338-40-4)
EPA Substance Registry System: (2R,3S,6R)-1-benzyloxycarbonyl-3-(tert-butyldimethylsilyloxy)-6-(2-(chloromethyl)allyl)-2-methylpiperidine(1242338-40-4)

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: 1242338-40-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242338-40-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,3,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1242338-40:
(9*1)+(8*2)+(7*4)+(6*2)+(5*3)+(4*3)+(3*8)+(2*4)+(1*0)=124
124 % 10 = 4
So 1242338-40-4 is a valid CAS Registry Number.

1242338-40-4Upstream product

18388-03-9 2-chloromethyl-3-trimethylsilyl-1-propene

1242338-40-4Downstream Products

1242338-40-4Relevant academic research and scientific papers

Synthesis of functionalized 3-hydroxypiperidines

Wijdeven, Marloes A.,Van Delft, Floris L.,Rutjes, Floris P.J.T.

, p. 5623 - 5636 (2010)

The synthetic versatility of three chemoenzymatically prepared hydroxypiperidine building blocks has been explored, resulting in a library of enantiopure functionalized piperidines. Key steps involved N-acyliminium ion-mediated CC-bond formation and cross-metathesis reactions, after which full deprotection led to the set of free 3-hydroxypiperidines.

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