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127075-48-3

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127075-48-3 Usage

General Description

Piperidin-2-ylmethyl trifluoromethanesulfonate is a chemical compound that is commonly used as a reagent in organic synthesis. It is a derivative of piperidine, a heterocyclic amine commonly found in natural products and pharmaceuticals. The trifluoromethanesulfonate group, also known as triflate, is a versatile leaving group that can be easily displaced in various chemical reactions. This reactivity makes piperidin-2-ylmethyl trifluoromethanesulfonate useful for the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and materials. Its high reactivity and versatility make it a valuable tool for synthetic chemists in the development of new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 127075-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,7 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127075-48:
(8*1)+(7*2)+(6*7)+(5*0)+(4*7)+(3*5)+(2*4)+(1*8)=123
123 % 10 = 3
So 127075-48-3 is a valid CAS Registry Number.

127075-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name piperidin-2-ylmethyl trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names HT1007

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:127075-48-3 SDS

127075-48-3Downstream Products

127075-48-3Relevant articles and documents

Bicyclic β-sultams: Synthesis from monocyclic β-aminothiols and some properties

Schwenkkraus,Otto

, p. 93 - 97 (1990)

The cyclamine methanethiols 7 are prepared from the corresponding alcohols 3 and oxidatively transformed by treatment with chlorine into the cyclic substituted taurinechlorides 8. Upon treatment with bases, 8 is cyclized yielding the bicyclic β-sultams 9. Some spectroscopic properties and the solvolysis of 9 are briefly discussed.

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