ChemicalBook--->CAS DataBase List--->29823-21-0

29823-21-0

29823-21-0 Structure

29823-21-0 Structure
IdentificationBack Directory
[Name]

8-BROMOOCTANOIC ACID ETHYL ESTER
[CAS]

29823-21-0
[Synonyms]

DK723
Nsc100182
SEMAGLUTIDE INT
8-bromodecanoate
Ethyl 8-bromooctanoat
ETHYL W-BROMOOCTANOATE
ETHYL 8-BROMOOCTANOATE
Ethyl-8-bromoocatnoate
Ethyl 8-bromoocatanoate
8-Bromooctanoic Ethylester
ETHYL OMEGA-BROMOOCTANOATE
Ethyl-8-broMooctanoic acid
8-CAPRYLIC ACID ETHYL ESTER
Ethyl 8-broMooctanoate, 98%+
8-Bromocaprylic acid ethyl este
ethyl 7-bromoheptanecarboxylate
8-Bromocaprylic acid ethyl ester
8-BroMooCLanoic Acid Ethyl Ester
8-BROMOOCTANOIC ACID ETHYL ESTER
Octanoic acid,8-bromo-, ethyl ester
8-Bromooctanoic Acid Ethyl Ester 99%
8-BROMOOCTANOIC ACID ETHYL ESTER ISO 9001:2015 REACH
8-bromo-Octanoic acid ethyl ester (6CI 7CI 8CI 9CI ACI)
Octanoic acid, 8-bromo-, ethyl ester (6CI, 7CI, 8CI, 9CI, ACI)
[EINECS(EC#)]

608-417-5
[Molecular Formula]

C10H19BrO2
[MDL Number]

MFCD00045057
[MOL File]

29823-21-0.mol
[Molecular Weight]

251.16
Chemical PropertiesBack Directory
[Boiling point ]

123°C/ 3mm
[density ]

1.194
[refractive index ]

1.458
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO (Slightly), Ethyl Acetate (Slightly)
[form ]

Oil
[color ]

Clear Colourless
[InChI]

InChI=1S/C10H19BrO2/c1-2-13-10(12)8-6-4-3-5-7-9-11/h2-9H2,1H3
[InChIKey]

UBTQVPMVWAEGAC-UHFFFAOYSA-N
[SMILES]

C(OCC)(=O)CCCCCCCBr
[LogP]

3.809
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H227
[Precautionary statements ]

P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235
[Hazard Codes ]

Xi
[REACH Registrations]

Active
[HazardClass ]

IRRITANT
[HS Code ]

2915907098
Hazard InformationBack Directory
[Uses]

Ethyl 8-bromooctanoate(cas:29823-21-0) is a useful research reagent for organic synthesis and other chemical processes.
[Synthesis]

The synthesis method of ethyl 8-bromooctanoate: 1, 6-dibromohexane initial raw material is firstly used for carrying out substitution reaction with diethyl malonate to generate 2- (6-bromohexyl) diethyl malonate, and then ester hydrolysis and decarboxylation reaction are carried out to obtain the 8-bromooctanoic acid; and finally, esterification reaction is carried out to generate the compound 8-bromoethyl octanoate.synthesis of ethyl 8-bromooctanoate
[Toxics Screening Level]

The initial threshold screening level (ITSL) for ethyl-8-bromooctanoate is 0.1 μg/m3 based on an annual averaging time.
[References]

[1] Tetrahedron Letters, 2001, vol. 42, # 2, p. 301 - 303
[2] Patent: US2003/228275, 2003, A1. Location in patent: Page 42
[3] Patent: US2003/229009, 2003, A1. Location in patent: Page 38
[4] Journal of Medicinal Chemistry, 2002, vol. 45, # 3, p. 563 - 566
[5] Synthesis, 1998, # 11, p. 1662 - 1669
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 8-bromooctanoate(29823-21-0)1HNMR
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