2-Bromo-3',4'-(methylenedioxy)propiophenone

2-Bromo-3',4'-(methylenedioxy)propiophenone 구조식 이미지
카스 번호:
52190-28-0
상품명:
2-Bromo-3',4'-(methylenedioxy)propiophenone
동의어(영문):
Bromo-3′ , 4′ - (methylenedioxy);3',4'-Methylenedioxy-α-broMopropiophenone;3',4'-Methylenedioxy-α-broMopropiophenone;2-Bromo-3',4'-(methylenedioxy)propiophenone;1-(1,3-benzodioxol-5-yl)-2-bromopropan-1-one;1-(1,3-Benzodioxol-5-yl)-2-broMo-1-propanone;1-Propanone, 1-(1,3-benzodioxol-5-yl)-2-bromo-;1-(benzo[d][1,3]dioxol-5-yl)-2-bromopropan-1-one;Name 2-Bromo-3',4'-(methylenedioxy)propiophenone;Ascorbyl Pa1-(benzo[d][1,3]dioxol-5-yl)-2-bromopropan-1-onelmitate
CBNumber:
CB6966513
분자식:
C10H9BrO3
포뮬러 무게:
257.08
MOL 파일:
52190-28-0.mol

2-Bromo-3',4'-(methylenedioxy)propiophenone 속성

끓는 점
345.7±42.0 °C(Predicted)
밀도
1.584±0.06 g/cm3(Predicted)
용해도
Chloroform: Soluble; DMSO: 1 mg/mL*; Ethanol: 1 mg/mL
물리적 상태
결정성 고체
InChI
InChI=1S/C10H9BrO3/c1-6(11)10(12)7-2-3-8-9(4-7)14-5-13-8/h2-4,6H,5H2,1H3
InChIKey
NTPQGLLTGPTOAA-UHFFFAOYSA-N
SMILES
C(C1=CC=C2OCOC2=C1)(=O)C(Br)C
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
그림문자(GHS): GHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H314 피부에 심한 화상과 눈에 손상을 일으킴 피부부식성 또는 자극성물질 구분 1A, B, C 위험 GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P330+P331 삼켰다면 입을 씻어내시오. 토하게 하려 하지 마시오.
P303+P361+P353 피부(또는 머리카락)에 묻으면 오염된 모든 의복은 벗거나 제거하시오 피부를 물로 씻으시오/샤워하시오.
P363 다시 사용전 오염된 의류는 세척하시오.
P405 밀봉하여 저장하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.

2-Bromo-3',4'-(methylenedioxy)propiophenone C화학적 특성, 용도, 생산

화학적 성질

Pale Yellow Solid

용도

1-(benzo[d][1,3]dioxol-5-yl)-2-bromopropan-1-one (2-Bromo-3',4'-(methylenedioxy)propiophenone) can be used in the preparation of antifungal agents and MDMA analogs.

Synthesis

Bromine (10.0 mmol) was added to a solution of the ketone (10.0 mmol) in Et2O (25 mL). The solution was stirred for 30 min (until the color of the solution changed from red to light-yellow). Then, the reaction was quenched with water (10 mL), and the mixture was diluted with Et2O (25 mL). The organic layer was washed with a saturated solution of aqueous NaHCO3 (30 mL), a saturated solution of aqueous Na2S2O3 (30 mL), and brine (30 mL), and then it was dried over MgSO4, filtered, and concentrated. The α-bromoketone was purified by flash chromatography on silica gel. 2-Bromo-3',4'-(methylenedioxy)propiophenone [52190-28-0]. This compound was prepared according to the General Procedure from 3,4-methylenedioxypropiophenone (1.78 g, 10.0 mmol). The product was obtained as a white solid (eluted with 50% CH2Cl2 in hexanes; 2.13 g, 82% yield). 1H NMR (CDCl3, 500 MHz) δ 7.64 (d, J= 8.0 Hz, 1H), 7.49 (s, 1H), 6.87 (d, J= 8.0 Hz, 1H), 6.07 (s, 2H), 5.21 (q, J= 7.0 Hz, 1H), 1.88 (d, J= 7.0 Hz, 3H).1-(benzo[d][1,3]dioxol-5-yl)-2-bromopropan-1-one synthesis

2-Bromo-3',4'-(methylenedioxy)propiophenone 준비 용품 및 원자재

원자재

준비 용품


2-Bromo-3',4'-(methylenedioxy)propiophenone 공급 업체

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