Cas 1242338-65-3,(2R,3S,6R)-1-benzyloxycarbonyl-3-hydroxy-2-methyl-6-(propa-1,2-dienyl)piperidine

1242338-65-3

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Basic information

Product Name: (2R,3S,6R)-1-benzyloxycarbonyl-3-hydroxy-2-methyl-6-(propa-1,2-dienyl)piperidine
Synonyms:
CAS NO:1242338-65-3
Molecular Formula:
Molecular Weight: 287.359
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-hydroxy-2-methyl-6-(propa-1,2-dienyl)piperidine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,6R)-1-benzyloxycarbonyl-3-hydroxy-2-methyl-6-(propa-1,2-dienyl)piperidine(1242338-65-3)
EPA Substance Registry System: (2R,3S,6R)-1-benzyloxycarbonyl-3-hydroxy-2-methyl-6-(propa-1,2-dienyl)piperidine(1242338-65-3)

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: 1242338-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242338-65-3 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, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1242338-65:
(9*1)+(8*2)+(7*4)+(6*2)+(5*3)+(4*3)+(3*8)+(2*6)+(1*5)=133
133 % 10 = 3
So 1242338-65-3 is a valid CAS Registry Number.

1242338-65-3Upstream product

13361-64-3 trimethyl(propargyl)silane

1242338-65-3Downstream Products

1242338-65-3Relevant academic research and scientific papers

Synthesis of functionalized 3-hydroxypiperidines

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

experimental part, p. 5623 - 5636 (2010/10/02)

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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