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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 701생성일: 2026년 10월 25일

메틸아세토아세트산에틸에스테르

메틸아세토아세트산에틸에스테르 · 에틸 2-메틸아세토아세트산 · Ethyl 2-methyl-3-oxobutanoate · Butanoic acid, 2-methyl-3-oxo-, ethyl ester · 2-Methylacetoacetate · Ethyl methylacetoacetate · Ethyl 2-methylacetacetate · Acetoacetic acid, 2-methyl-, ethyl ester

https://huagongshe.com/ko/chemical/701

메틸아세토아세트산에틸에스테르 분자 구조식

식별자 및 물리적 특성

CAS No.609-14-3
분자식C7H12O3
평균 분자량144.17 g/mol
단동위원소 질량144.07864424 g/mol
SMILESCCOC(=O)C(C)C(C)=O
InChIKeyFNENWZWNOPCZGK-UHFFFAOYSA-N
PubChem CID701
ChEMBLCHEMBL31596
EC No.210-179-9
DTXSIDDTXSID2033493
현지명메틸아세토아세트산에틸에스테르

화학 및 물리적 성질

XLogP0.9
극성 표면적43.4
수소 결합 공여자 수0
수소 결합 수용자 수3
회전 가능 결합 수4
무거운 원자 수10
형식 전하0
복잡도140
녹는점-45 °C
끓는 점187 °C (lit.)
밀도1.019 g/mL at 25 °C (lit.)
굴절률n20/D 1.418(lit.)
인화점145 °F
저장 조건Inert atmosphere,Room Temperature
용해도클로로포름(약간 용해됨), 메탄올(약간 용해됨)
pKa(산도 계수)11.98±0.46(Predicted)
물리적 상태액체
비중1.019
색상무색~황색으로 투명함
용해도섞일 수 없음
BRN1071742
InChI1S/C7H12O3/c1-4-10-7(9)5(2)6(3)8/h5H,4H2,1-3H3
InChIKeyFNENWZWNOPCZGK-UHFFFAOYSA-N
SMILESCCOC(=O)C(C)C(C)=O
LogP(분배 계수)1.063 (est)
NISTButanoic acid, 2-methyl-3-oxo-, ethyl ester(609-14-3)
EPAButanoic acid, 2-methyl-3-oxo-, ethyl ester (609-14-3)

화학적 성질

clear colorless to yellow liquid

안전 및 규제

GHS 분류WarningH227 (25%): Combustible liquid [Warning Flammable liquids]P210, P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 4 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보Chemical: Butanoic acid, 2-methyl-3-oxo-, ethyl ester
Hazard Classes and CategoriesFlam. Liq. 4 (25%)
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
운송 번호(UN)1993
관세 코드29182300
안전 문구(S)24/25
저장 분류10 - Combustible liquids

용도

용도

Ethyl 2-methylacetoacetate is used in Japp-Klingemann reaction to prepare hydrazones from beta-keto acid and aryl diazonium salts. It is used as a precursor involved in the synthesis of ethylpyruvate phenylhydrazone via reaction with benzenediazonium chloride.