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Ethyl 6-(acetylamino)-3,5,7-trioxo-1-phenylhexahydro-1H-pyrrolizine-2-carboxylate is a complex organic compound with the molecular formula C15H18N2O5. It is a derivative of pyrrolizine, a heterocyclic compound with a five-membered ring containing two nitrogen atoms. The molecule features a phenyl group attached to the pyrrolizine ring, and an acetylamino group at the 6-position. The structure also includes three oxygen atoms, which contribute to the compound's trioxide functionality. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds, due to its unique structure and reactivity.

7225-39-0

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7225-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7225-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7225-39:
(6*7)+(5*2)+(4*2)+(3*5)+(2*3)+(1*9)=90
90 % 10 = 0
So 7225-39-0 is a valid CAS Registry Number.

7225-39-0SDS

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 ethyl 6-acetamido-3,5,7-trioxo-1-phenyl-2,8-dihydro-1H-pyrrolizine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Dodeca-2,4,6,8,10-pentaen-saeure

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:7225-39-0 SDS

7225-39-0Downstream Products

7225-39-0Relevant academic research and scientific papers

A general and practical synthesis of linear conjugated pentaenoic acids

Souto, Andre A.,Ulises Acuna,Amat-Guerri, Francisco

, p. 5907 - 5910 (1994)

An easy and practical synthesis of all(E)-2,4,6,8,10-dodecapentaenoic acid (1), all(E)-5,7,9,11,13-pentadecapentaenoic acid (2), all(E)-8,10,12,14,16- octadecapentaenoic acid (3) and its (8Z)-isomer (4) by application of the Wittig olefination reaction is described.

The fumagillin biosynthetic gene cluster in Aspergillus fumigatus encodes a cryptic terpene cyclase involved in the formation of β-trans-bergamotene

Lin, Hsiao-Ching,Chooi, Yit-Heng,Dhingra, Sourabh,Xu, Wei,Calvo, Ana M.,Tang, Yi

, p. 4616 - 4619 (2013)

Fumagillin 1 is a meroterpenoid from Aspergillus fumigatus that is known for its anti-angiogenic activity by binding to human methionine aminopeptidase 2. The genetic and molecular basis for biosynthesis of 1 had been an enigma despite the availability of the A. fumigatus genome sequence. Here, we report the identification and verification of the fma gene cluster, followed by characterization of the polyketide synthase and acyltransferase involved in biosynthesis of the dioic acid portion of 1. More significantly, we uncovered the elusive β-trans-bergamotene synthase in A. fumigatus as a membrane-bound terpene cyclase.

Direct conversion of polyconjugated compounds into their corresponding carboxylic acids by Acetobacter aceti

Pini, Elena,Bertacche, Vittorio,Molinari, Francesco,Romano, Diego,Gandolfi, Raffaella

, p. 8638 - 8641 (2008/12/21)

The conversion of polyconjugated aldehydes or alcohols into their corresponding acids was carried out using Acetobacter aceti. The analytical results were compared with those of the acids chemically obtained using a Horner-Wittig reaction.

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