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24095-40-7

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24095-40-7 Usage

General Description

4-Isocyanato-1-(trifluoroacetyl)piperidine is a chemical compound with the molecular formula C8H10F3NO2. It features an isocyanate group, known for their reactivity and utility in creating various chemical products like polyurethane foams, and a trifluoroacetyl group, which is a chemical entity containing exactly one trifluoroacetyl (COC(F)(F)F) group. Piperidine, a common organic compound in pharmaceuticals and fine chemicals, is also part of its structure. However, specific data about this compound's properties, such as its physical state, boiling point, melting point, toxicity levels, storage conditions, or applications, is not readily available in the literature, likely indicating it is not a widely used or studied chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 24095-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24095-40:
(7*2)+(6*4)+(5*0)+(4*9)+(3*5)+(2*4)+(1*0)=97
97 % 10 = 7
So 24095-40-7 is a valid CAS Registry Number.

24095-40-7SDS

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 [4-(aminomethyl)phenyl]-phenylmethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-benzoylbenzylamine 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:24095-40-7 SDS

24095-40-7Downstream Products

24095-40-7Relevant articles and documents

Catalytic Staudinger Reduction at Room Temperature

Lenstra, Danny C.,Wolf, Joris J.,Mecinovi?, Jasmin

, p. 6536 - 6545 (2019/05/24)

We report an efficient catalytic Staudinger reduction at room temperature that enables the preparation of a structurally diverse set of amines from azides in excellent yields. The reaction is based on the use of catalytic amounts of triphenylphosphine as a phosphine source and diphenyldisiloxane as a reducing agent. Our catalytic Staudinger reduction exhibits a high chemoselectivity, as exemplified by reduction of azides over other common functionalities, including nitriles, alkenes, alkynes, esters, and ketones.

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