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2207-52-5

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2207-52-5 Usage

Main Use

Building block in pharmaceuticals, agrochemicals, and organic compounds synthesis

Parent Compound

Piperidine, a heterocyclic amine

Derivative

It is derived from piperidine

Functional Groups

Two ester groups attached to the piperidine ring

Versatility

Serves as a versatile intermediate for synthesizing complex organic molecules

Reactivity

Exhibits significant reactivity in organic chemistry applications

Importance

Plays a crucial role in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 2207-52-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2207-52:
(6*2)+(5*2)+(4*0)+(3*7)+(2*5)+(1*2)=55
55 % 10 = 5
So 2207-52-5 is a valid CAS Registry Number.

2207-52-5SDS

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 dimethyl piperidine-2,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names Piperidin-2,5-dicarbonsaeure-dimethylester

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:2207-52-5 SDS

2207-52-5Relevant articles and documents

Preparation of differentiated diamides of 4,5,6,7-tetrahydropyrazolo[1,5-a] pyridine-2,6- and -3,6-dicarboxylic acids suitable for parallel synthesis

Erdmane,Zemribo

scheme or table, p. 811 - 816 (2012/03/22)

1,3-Dipolar cycloaddition of a bicyclic sydnone to a propargylic acid amide affords 4,5,6,7-tetra-hydropyrazolo[1,5-a]pyridine-2,6- and -3,6-dicarboxylic acid monoamides which are further converted to corresponding differentiated diamides.

Synthesis of trans-7-Hydroxymethyl-2-(2-benzisoxazol-3-yl)octahydro-2H-pyridopyrazine

Urban, Frank J.

, p. 857 - 862 (2007/10/02)

An efficient synthesis of trans-7-hydroxymethyl-2-(2-benzisoxazol-3-yl)octahydro-2H-pyridopyrazine 2 is presented which relies on the equilibration of cis-dimethyl piperidinedicarboxylate followed by alkylation with phthalimidoethyl triflate.

Synthesis of tabtoxinine δ lactam

Lee,Rapoport

, p. 3491 - 3495 (2007/10/04)

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