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14842-41-2

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14842-41-2 Usage

Description

(S,S)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,6,8,12-tetrone is a complex organic compound with a unique cyclic structure. It is characterized by its diazatricyclic core and four ketone functional groups, which contribute to its chemical properties and potential applications.

Uses

Used in Chemical Synthesis:
(S,S)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,6,8,12-tetrone is used as a key intermediate in the synthesis of various complex organic molecules, particularly those with potential pharmaceutical or chemical applications. Its unique structure and functional groups make it a valuable building block for the development of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (S,S)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,6,8,12-tetrone is used as a starting material for the development of novel drugs. Its structural features and reactivity can be exploited to design and synthesize new therapeutic agents with potential applications in various medical fields.
Used in Material Science:
(S,S)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,6,8,12-tetrone can also be utilized in the field of material science, where its unique properties may contribute to the development of new materials with specific characteristics. For example, its potential use in the synthesis of novel polymers or as a component in advanced composite materials could be explored.
Used in Analytical Chemistry:
Due to its distinct chemical structure, (S,S)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,6,8,12-tetrone may find applications in analytical chemistry as a chiral reference compound or as a component in the development of new chiral stationary phases for chromatographic separations.

Check Digit Verification of cas no

The CAS Registry Mumber 14842-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,4 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14842-41:
(7*1)+(6*4)+(5*8)+(4*4)+(3*2)+(2*4)+(1*1)=102
102 % 10 = 2
So 14842-41-2 is a valid CAS Registry Number.

14842-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (5aS,10aS)-Tetrahydrodipyrrolo[1,2-a:1',2'-d]pyrazine-3,5,8,10(2H,5aH)-tetraone

1.2 Other means of identification

Product number -
Other names (5aS,10aS)-1,2,5a,6,7,10a-hexahydrodipyrrolo[1,3-c:1',3'-f]pyrazine-3,5,8,10-tetrone

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:14842-41-2 SDS

14842-41-2Relevant articles and documents

Five- and six-membered ring opening of pyroglutamic diketopiperazine

Parrish, Dennis A.,Mathias, Lon J.

, p. 1820 - 1826 (2007/10/03)

A variety of ring-opening reactions of pyroglutamic diketopiperazine at both the five-membered and six-membered rings is described. Mild, basic conditions facilitate nucleophilic attack by amines at the diketopiperazine carbonyls giving pyroglutamides in excellent yield. Reaction with nucleophiles under acidic conditions give bis-glutamate derivatives of 2,5-diketopiperazine (DKP). These reactions provide simple, two-step sequences to pyroglutamides and symmetrical diketopiperazines from commercial pyroglutamic acid with control of product dictated by reaction conditions, catalyst, and nucleophile.

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