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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 70684생성일: 2026년 10월 27일

Bromopyruvic Acid

BROMOPYRUVIC ACID · 3-BROMO-2-OXOPROPANOIC ACID · 3-bromopyruvate · 3-BROMOPYRUVIC ACID · bromopyruvate · 3-BROMO-2-OXOPROPIONIC ACID · 2-Oxo-3-bromopropanoic acid · beta-bromopyruvicacid

https://huagongshe.com/ko/chemical/70684

Bromopyruvic Acid 분자 구조식

식별자 및 물리적 특성

CAS No.1113-59-3
분자식C3H3BrO3
평균 분자량166.96 g/mol
단동위원소 질량165.92655606 g/mol
SMILESO=C(O)C(=O)CBr
InChIKeyPRRZDZJYSJLDBS-UHFFFAOYSA-N
PubChem CID70684
ChEMBLCHEMBL177837
ChEBICHEBI:131461
EC No.214-206-5
DTXSIDDTXSID7040940

화학 및 물리적 성질

XLogP0.5
극성 표면적54.4
수소 결합 공여자 수1
수소 결합 수용자 수3
회전 가능 결합 수2
무거운 원자 수7
형식 전하0
복잡도98.4
녹는점77-82 °C
끓는 점223.4±23.0 °C(Predicted)
밀도1.7314 (rough estimate)
굴절률1.4650 (estimate)
저장 조건2-8°C
용해도물: 용해성1g/10mL, 투명, 무색
물리적 상태백색 결정성 고체
pKa(산도 계수)1.84±0.54(Predicted)
색상흰색에서 거의 흰색
용해도물, 디메틸 설폭사이드, 에틸 아세테이트 및 물에 용해됩니다.
BRN1746786
InChIInChI=1S/C3H3BrO3/c4-1-2(5)3(6)7/h1H2,(H,6,7)
InChIKeyPRRZDZJYSJLDBS-UHFFFAOYSA-N
SMILESC(O)(=O)C(=O)CBr
EPAPropanoic acid, 3-bromo-2-oxo- (1113-59-3)

화학적 성질

Off-white solid

안전 및 규제

GHS 분류DangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 48 reports by companies from 6 notifications to the ECHA C&L Inventory.
Hazard Classes and CategoriesSkin Corr. 1B (100%)
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
RTECS 번호UZ0840000
운송 번호(UN)UN 3261 8/PG 2
관세 코드29183000
위험 문구(R)34-20/21/22
위험 표시C
안전 문구(S)26-36/37/39-45-27
포장분류II
위험 등급8Eye Dam. 1Skin Corr. 1B
F 고인화성물질19-21
위험 참고 사항Corrosive
저장 분류8A - Combustible corrosive hazardous materials

용도

용도

Bromopyruvic Acid is a synthetic brominated derivative of pyruvic acid. Bromopyruvic Acid maybe a potential treatment for certain types of cancer as it has shown to be effective at eliminating aggress ive liver tumors.

일반 설명

Bromopyruvic acid is an affinity label for cysteine residues. It acts as cross-linker between nucleic acids and proteins. Kinetics of inactivation of pancreatic ribonuclease A by bromopyruvic acid has been investigated.

제조 및 합성 방법

제조 방법

Synthesis method of 3-bromopyruvic acid: add a little concentrated sulfuric acid and solvent dichloromethane to pyruvic acid in a reaction flask, add bromine dropwise for about 3.5h and stir, a white precipitate is produced, then continue to stir for 1h, dilute with cyclohexane and petroleum ether, then cool the reaction mixture to get crystals, filter, wash with petroleum ether and dry to get the finished product of 3-bromopyruvic acid.