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4-Hydroxy-4-(1H-imidazol-4-yl)piperidine-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173469-30-2

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173469-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173469-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173469-30:
(8*1)+(7*7)+(6*3)+(5*4)+(4*6)+(3*9)+(2*3)+(1*0)=152
152 % 10 = 2
So 173469-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H21N3O3/c1-12(2,3)19-11(17)16-6-4-13(18,5-7-16)10-8-14-9-15-10/h8-9,18H,4-7H2,1-3H3,(H,14,15)

173469-30-2SDS

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 tert-butyl 4-hydroxy-4-(1H-imidazol-5-yl)piperidine-1-carboxylate

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

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

More Details:173469-30-2 SDS

173469-30-2Downstream Products

173469-30-2Relevant academic research and scientific papers

Two Novel Syntheses of the Histamine H3 Antagonist Thioperamide

Lange, Jos H. M.,Wals, Henri C.,Hoogenband, Adri van den,Kuilen, Aalt van de,Hartog, Jack A. J. den

, p. 13447 - 13454 (1995)

The previously described route for the synthesis of the histamine H3 antagonist thioperamide 3 has been improved considerably.Furthermore, two straightforward novel synthetic routes towards 3 are described herein.The last synthetic route (Scheme 3) is preferable as it is very suitable for the production of multigram quantities of thioperamide 3.

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