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62414-68-0

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62414-68-0 Usage

General Description

(R)-Piperidin-3-ol, also known as (R)-3-hydroxypiperidine, is a chemical compound with the molecular formula C5H11NO. It is a chiral molecule with a piperidine ring and a hydroxyl group, and it exists in two enantiomeric forms, with (R)-Piperidin-3-ol being the right-handed form. (R)-Piperidin-3-ol has been used in the synthesis of various pharmaceuticals and organic compounds. It is also used as a building block in the production of agrochemicals, dyes, and other specialty chemicals. Additionally, research has shown that (R)-Piperidin-3-ol has potential pharmacological properties, such as anti-inflammatory and analgesic effects, making it a promising candidate for drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 62414-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,1 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62414-68:
(7*6)+(6*2)+(5*4)+(4*1)+(3*4)+(2*6)+(1*8)=110
110 % 10 = 0
So 62414-68-0 is a valid CAS Registry Number.

62414-68-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-piperidin-3-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62414-68-0 SDS

62414-68-0Relevant articles and documents

A practical and enantiospecific synthesis of (-)-(R)- and (+)-(S)-piperidin-3-ols

Babu, Meruva Suresh,Raghunadh, Akula,Ramulu, Konda,Dahanukar, Vilas H.,Syam Kumar, Unniaran K.,Dubey, P. Kumar

, p. 1507 - 1515 (2015/02/19)

A highly enantiospecific, azide-free synthesis of (-)-(R)- and (+)-(S)-piperidin-3-ol in excellent yield was developed. The key step of the synthesis involves the enantiospecific ring openings of enantiomerically pure (R)- and (S)-2-(oxiran-2-ylmethyl)-1H-isoindole-1,3(2H)-diones with the diethyl malonate anion and subsequent decarboxylation.

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