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105955-84-8

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105955-84-8 Usage

General Description

1-Piperidinebutanal, 4-(hydroxydiphenylmethyl)- is an organic compound that is categorized under the chemical class of Piperidines. It is recognized by various names, including Diphenydol, and it has a molecular weight of 379.44 g/mol. This chemical appears as a crystalline substance and is commonly used in the preparation of pharmaceutical compounds due to its structural properties. Properties like low melting point and high boiling point make it stable under various conditions. Like with all chemicals, care should be taken while handling this compound due to potential risks and hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 105955-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,5 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105955-84:
(8*1)+(7*0)+(6*5)+(5*9)+(4*5)+(3*5)+(2*8)+(1*4)=138
138 % 10 = 8
So 105955-84-8 is a valid CAS Registry Number.

105955-84-8SDS

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 4-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]butanal

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:105955-84-8 SDS

105955-84-8Downstream Products

105955-84-8Relevant articles and documents

Synthesis of terfenadine carboxylate

Patel, Sunil,Waykole, Liladhar,Repic, Oljan,Chen, Kau-Ming

, p. 4699 - 4710 (2007/10/03)

A synthesis of terfenadine carboxylate, 1, a metabolite of terfenadine 2, is described. In the key step, the sodium salt of 2-(4-bromo-phenyl)-2-methylpropionic acid, 7, was lithiated via a metal-halogen exchange using t-BuLi and subsequently condensed with 4-[4-(hydroxydiphenylmethylpiperidin-1-yl]butyraldehyde, 5, to afford terfenadine carboxylate, 1.

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