Dimethyl fluoromalonate

Dimethyl fluoromalonate 구조식 이미지
카스 번호:
344-14-9
상품명:
Dimethyl fluoromalonate
동의어(영문):
METHYL 2-FL;DIMETHYL FLUOROMALONATE;Dimethyl 2-fluoromalonate;Dimethylfluoromalonate97%;Dimethyl fluoromalonate 97%;fluoro-malonicaciddimethyles;imethyl2-fluoropropanedioate;Dimethyl 2-fluoromalonate 97%;Dimethyl 2-fluoropropanedioate;fluoro-malonicaciddimethylester
CBNumber:
CB2216739
분자식:
C5H7FO4
포뮬러 무게:
150.11
MOL 파일:
344-14-9.mol

Dimethyl fluoromalonate 속성

끓는 점
76 °C
밀도
1.4g/ml
굴절률
1.4032
인화점
111-112°C/45mm
산도 계수 (pKa)
10.35±0.46(Predicted)
물리적 상태
고체
물리적 상태
단단한 모양
색상
Colourless to off-white / liquid
BRN
1768414
CAS 데이터베이스
344-14-9(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,C
위험 카페고리 넘버 34
안전지침서 26-36/37/39-45-23 2636/37/3945-20
유엔번호(UN No.) 3265
위험 참고 사항 Toxic
위험 등급 8
포장분류 II
HS 번호 29171900
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
H318 눈에 심한 손상을 일으킴 심한 눈 손상 또는 자극성 물질 구분 1 위험 GHS hazard pictograms P280, P305+P351+P338, P310
예방조치문구:
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.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P405 밀봉하여 저장하시오.
NFPA 704
1
3 0

Dimethyl fluoromalonate MSDS


Dimethyl fluoromalonate

Dimethyl fluoromalonate C화학적 특성, 용도, 생산

화학적 성질

white to light yellow crystal powder

용도

Dimethyl 2-fluoromalonate is used as an intermediate in organic synthesis.

제조 방법

synthesis of dimethyl 2-fluoromalonate: Dimethyl malonate (19.8 g, 0.15 mol) and Cu(NO3)2·2.5H2O (3.50 g, 15 mmol) were dissolved in acetonitrile (85 mL), the mixture was cooled to 0–5 °C and stirred at 650 rpm using an overhead stirrer. After purging the system with N2 for 5 minutes, fluorine gas (20% v/v in N2, 50 mL min-1 , 170 mmol) was introduced into the reaction mixture for 7 h. After purging with nitrogen for 20 minutes, the solvent was removed in vacuo and the residue was partitioned between water (30 mL) and ethyl acetate (20 mL). The aqueous phase was extracted with ethyl acetate (2 × 20 mL) and the combined organic layer was washed with saturated brine (20 mL). After drying over sodium sulphate, the solvent was evaporated under reduced pressure to give dimethyl 2-fluoromalonate (21.8 g, 97% yield, 95% purity) as a colourless oil;
IR (neat, cm-1 ) 2962, 1748, 1438, 1250, 1206, 1112, 1016; δH (CDCl3, 400 MHz) 3.85 (6H, s, CH3), 5.31 (1H, d, 2 JHF 48.0, CHF); δF (CDCl3, 376 MHz): -195.73 (d, 2 JHF 48.0, CH–F); δC (CDCl3, 100 MHz) 53.48 (CH3), 85.19 (d, 1 JCF 197.2, C–F), 164.39 (d, 2 JCF 24.0, CvO); m/z (EI+ ) 150 (3%, [M]+ ), 119 (42%, [M-OMe]+ ), 91 (73%, [M-COOMe]+ ), 59 (100%, [COOMe]+ ).

Dimethyl fluoromalonate 준비 용품 및 원자재

원자재

준비 용품


Dimethyl fluoromalonate 공급 업체

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