135501-61-0

Basic information

• Product Name: cis-3,4-Dihydroxypiperidine
• Synonyms: cis-3,4-Dihydroxypiperidine;(3S,4R)-Piperidine-3,4-diol
• CAS NO: 135501-61-0
• Molecular Formula: C₅H₁₁NO₂
• Molecular Weight: 117.15
• Product Categories: pharmacetical
• Mol File: 135501-61-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 233.4°Cat760mmHg
• Flash Point: 129.3°C
• Appearance: /
• Density: 1.214g/cm³
• Vapor Pressure: 0.0104mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: cis-3,4-Dihydroxypiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: cis-3,4-Dihydroxypiperidine(135501-61-0)
• EPA Substance Registry System: cis-3,4-Dihydroxypiperidine(135501-61-0)

Safety Data

• Hazardous Substances Data: 135501-61-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C5H11NO2/c7-4-1-2-6-3-5(4)8/h4-8H,1-3H2/t4-,5+/m1/s1

Upstream product

• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 170553-85-2 2′-deoxy-1′-O-methyl-5′-azido-D-ribofuranose 
• 10437-39-5 methyl 2-deoxy-5-O-(p-toluenesulfonyl)-α,β-D-erythro-pentofuranoside 

Downstream Products

• 951766-53-3 (3R,4S)-1-tert-butoxycarbonyl-3,4-dihydroxypiperidine 

Relevant articles and documents

2-Deoxyribose as a rich source of chiral 5-carbon building blocks

(Chemical Equation Presented) We have developed concise routes to a number of useful chiral 5-carbon synthetic building blocks using readily available O-1-methyl-2-deoxyribose as starting material. Novel transformations include the use of indium triflate

NOVEL ALKYNE COMPOUNDS WITH AN MCH-ANTAGONISTIC ACTION AND MEDICAMENTS CONTAINING SAID COMPOUNDS

The invention relates to alkyne compounds of general formula (I), in which the groups and radicals A, B, W, X, Y, Z, R1 and R2 are defined as cited in claim 1. The invention also relates to medicaments containing at least one inventive alkyne. As a result of the antagonistic action against the MCH-receptor, the inventive medicaments are suitable for treating metabolic disorders and/or eating disorders, in particular adiposity and diabetes.

Palladium-mediated stereocontrolled reductive amination of azido sugars prepared from enzymatic aldol condensation: A general approach to the synthesis of deoxy aza sugars

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