Diethyl (trichloromethyl)phosphonate

Diethyl (trichloromethyl)phosphonate 구조식 이미지
카스 번호:
866-23-9
상품명:
Diethyl (trichloromethyl)phosphonate
동의어(영문):
Ro-30658;TIMTEC-BB SBB008195;DIETHYL TRICHLOROMETHYLPHOSPHONATE;diethyl trichloromethanephosphonate;Trichloromethylphosphonic acid diethyl;(Trichloromethyl)phosphonic acid diethyl;Diethyl (trichloromethyl)phosphonate 97%;Diethyl (Trichloromethyl)phosphonate >trichloromethyl-phosphonicacidiethylester;DIETHYL (TRICHLOROMETHYL)PHOSPHONATE, 97 %
CBNumber:
CB7725977
분자식:
C5H10Cl3O3P
포뮬러 무게:
255.46
MOL 파일:
866-23-9.mol

Diethyl (trichloromethyl)phosphonate 속성

끓는 점
130-131 °C/14 mmHg (lit.)
밀도
1.362 g/mL at 25 °C (lit.)
굴절률
n20/D 1.463(lit.)
인화점
>230 °F
저장 조건
2-8°C
물리적 상태
액체
색상
무색 내지 거의 무색
수용성
4.5g/L(25℃)
BRN
1210640
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38-22
안전지침서 26-36-60-36/37
유엔번호(UN No.) UN3278
WGK 독일 3
RTECS 번호 TA0988000
F 고인화성물질 9-21
위험 등급 6.1
포장분류 III
HS 번호 29319000
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P304+P340 흡입하면 신선한 공기가 있는 곳으로 옮기고 호흡하기 쉬운 자세로 안정을 취하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P405 밀봉하여 저장하시오.
NFPA 704
1
2 0

Diethyl (trichloromethyl)phosphonate C화학적 특성, 용도, 생산

화학적 성질

Colorless to Almost colorless clear liquid.

용도

Diethyl (trichloromethyl)phosphonate may be used in the synthesis of chlorovinyl phosphonates via reaction with aldehydes and ketones.

제조 방법

Diethyl trichloromethylphosphonate was also obtained from diethyltrimethylsilyl phosphite in 60 % yield, and from benzyldiethyl phosphite in the presence of dibenzoyl peroxide and an ultraviolet source in a radical induced reaction in 87 % yield (compared to 26 % without the dibenzoyl peroxide).

주요 응용

Diethyl trichloromethylphosphonate has been used as a carbenoid precursor in the reaction with Bu3B.
Diethyl trichloromethylphosphonate is used mainly in the synthesis of 1,1-dichloro-1-alkenes from carbonyl compounds via Horner–Wadsworth–Emmons (HWE)-type reactions.
Diethyl trichloromethylphosphonate reacts with olefins under Cu(I) or Fe(III) catalysis to give insertion of the olefinic substrate into one of the C–Cl bonds.

일반 설명

Addition reaction of diethyl (trichloromethyl)phosphonate to olefins by non-chain catalytic reactions catalyzed by copper amine complexes has been reported. Irradiation of diethyl (trichloromethyl)phosphonate in MeCN is reported to afford corresponding monoesters and olefins, via photochemical type II elimination reaction.

Diethyl (trichloromethyl)phosphonate 준비 용품 및 원자재

원자재

준비 용품


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