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Ethyl 7-bromoheptanoate CAS No. 29823-18-5 7-BROMOHEPTANOIC ACID ETHYL ESTER

Ethyl 7-bromoheptanoate CAS No. 29823-18-5 7-BROMOHEPTANOIC ACID ETHYL ESTER CAS NO.29823-18-5

Min.Order: 1 Kilogram
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Product Details

Keywords

Ethyl 7-bromoheptanoate
CAS No. 29823-18-5
7-BROMOHEPTANOIC ACID ETHYL ESTER

Quick Details

ProName: Ethyl 7-bromoheptanoate CAS No. 29823-...
CasNo: 29823-18-5
Molecular Formula: C9H17BrO2
Appearance: Colorless to pale yellow liquid
Application: Pharmaceutical Intermediate； Chemical...
DeliveryTime: c.a 1-2 weeks depending on the order d...
PackAge: 25KG/barrel , 200 KG/Drum or others ac...
Port: Qingdao/Beijing/Tianjin/Shanghai/Ningb...
ProductionCapacity: 30 Metric Ton/Month
Purity: 98%,99%
Storage: keep it sealed at cool dry ventilated ...
Transportation: Hazard Codes Xi Risk Statements 36/3...
LimitNum: 1 Kilogram

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Details

Ethyl 7-bromoheptanoate Basic information

Product Name:	Ethyl 7-bromoheptanoate
Synonyms:	Ethyl 7-bromoheptanoate 97%; ETHYL W-BROMOHEPTANOATE; ETHYL 7-BROMOHEPTANOATE; 7-BROMOHEPTANOIC ACID ETHYL ESTER; 7-BROMOHEPTANOIC ACID ETHYL ESTER 96+%; Tianeptine EP Impurity A
CAS:	29823-18-5
MF:	C9H17BrO2
MW:	237.13
EINECS:	249-883-6
Product Categories:	Pharmaceutical Intermediates;C8 to C9;Carbonyl Compounds;Esters
Mol File:	29823-18-5.mol

Ethyl 7-bromoheptanoate Chemical Properties

Safety Information

Chemical Properties

Colorless to pale yellow liquid

Uses

Ethyl 7-bromoheptanoate may be used in the following studies:As a starting material in the synthesis of benzyl 7-iodoheptanoate.

As one of the reactant in the synthesis of diethyl 7,7′-(2,5-diiodo-1,4-phenylene)bis(oxy)diheptanoate.
As one of the reagent in the synthesis of CarnDOD-7C, a carnitine-derived nitrone.
As an alkylating agent in the alkylation of ethyl 3-oxoglutarate to form 2-(6-ethoxycarbonylhexyl)-3-oxoglutarate.
Synthesis of 1-substituted cyclopentadiene by alkylating lithium cyclopentadienide.5

General Description

Ethyl 7-bromoheptanoate is a bromoester. It is used as an alkylating agent for organic compounds. It participates in the synthesis of ω-chain shortened prostaglandins.