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105973-51-1

105973-51-1

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105973-51-1 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 105973-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,7 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105973-51:
(8*1)+(7*0)+(6*5)+(5*9)+(4*7)+(3*3)+(2*5)+(1*1)=131
131 % 10 = 1
So 105973-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c14-12-7-4-8-13(10-12)9-11-5-2-1-3-6-11/h1-3,5-6,12,14H,4,7-10H2/p+1/t12-/m0/s1

105973-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl-3-piperidinol hydrochloride

1.2 Other means of identification

Product number -
Other names 1-benzylpiperidin-3-ol,hydrochloride

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

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

More Details:105973-51-1 SDS

105973-51-1Upstream product

105973-51-1Relevant articles and documents

Synthesis method of N-benzyl-3-hydroxypiperidine

-

Paragraph 0022; 0025-0026; 0029-0030; 0033, (2021/11/06)

The invention discloses a synthetic method of 3-hydroxypiperidine, and belongs to the technical field of organic synthesis. The method comprises the following steps: by taking 3-hydroxypiperidine as a starting raw material, selectively protecting hydroxyl by using an optimized silicon protection reagent, then conducting reacting with benzyl halide under a weak alkaline condition, finally, conducting deprotecting under an acidic condition to obtain N-benzyl-3-hydroxypiperidine hydrochloride, and performing alkaline dissociation to obtain N-benzyl-3-hydroxypiperidine. The synthesis method has the advantages of cheap and easily available raw materials and reagents, mild reaction conditions, simple operation and high yield, and is suitable for industrial production.

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