Dimethyl (1-Diazo-2-oxopropyl)phosphonate

Dimethyl (1-Diazo-2-oxopropyl)phosphonate 구조식 이미지
카스 번호:
90965-06-3
상품명:
Dimethyl (1-Diazo-2-oxopropyl)phosphonate
동의어(영문):
DIMETHYL (1-DIAZO-2-OXOPROPYL)PHOSPHONATE;Ohira-Bestmann reagent;1-Diazo-1-dimethoxyphosphoryl-propan-2-one;Dimethyl (acetyldiazomethyl)phosphonate;dimethyl 1-(1-diazo-2-oxopropyl)phosphonate;1-Diazoacetonylphosphonic Acid Dimethyl Ester;Dimethyl 1-Diazoacetonylphosphonate;Dimethyl (1-azoacetonyl)phosphonate;diMethyl(1-diazo-2-oxopropyl)phosphanate;dimethyl (2-oxopropanimidoyl)phosphonate
CBNumber:
CB8489377
분자식:
C5H9N2O4P
포뮬러 무게:
192.11
MOL 파일:
90965-06-3.mol

Dimethyl (1-Diazo-2-oxopropyl)phosphonate 속성

밀도
1.28
굴절률
n20/D1.352-1.354
인화점
2℃
저장 조건
2-8°C
용해도
에 용해됨클로로포름, 메탄올 (약간 용해됨)
물리적 상태
기름
색상
연한 노란색에서 노란색까지
Merck
14,1177
BRN
4247670
안정성
감광성
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F,Xn
위험 카페고리 넘버 11-20/21/22-36
안전지침서 16-26-36/37
유엔번호(UN No.) UN 1648 3 / PGII
WGK 독일 3
위험 등급 3
포장분류 II
HS 번호 29319090
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H225 고인화성 액체 및 증기 인화성 액체 구분 2 위험 GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
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.
NFPA 704
0
2 0

Dimethyl (1-Diazo-2-oxopropyl)phosphonate C화학적 특성, 용도, 생산

개요

Dimethyl (1-diazido-2-oxopropyl)phosphonate is a liquid-added organophosphorus flame retardant with good solubility with water, common organic solvents, and inorganic salts flame retardants, with excellent flame retardant properties, low price and low additive amount and other advantages.

화학적 성질

Light yellow liquid

주요 응용

Dimethyl (1-diazo-2-oxopropyl)phosphonate can be used as a reagent for the synthesis of:
Ethynyl compounds (alkynes) from aldehydes.
Isoquinoline and pyridine N-oxides by cyclization with oximes in the presence of Rh catalyst.
Dimethyl(diazomethyl)phosphonate through methanolysis, which is further employed as a reagent in the synthesis of enol ethers or alkynes.
Five-member heterocyclic scaffolds of pyrazoles, triazoles, and oxazoles via cycloaddition reaction and multicomponent reaction.

용도

Reagent for transformation of aldehydes to terminal alkynes and ketones to methyl enol ethers.

Synthesis

Dissolve NaH (0.67 g, 60% w/w, 16.75 mmol) in benzene (45 mL) and dry THF (15 mL). Cool the mixture on ice. A solution of dimethyl (2-oxopropyl) phosphonate (15.3 mmol) in dry benzene (15 mL) was added. A white solid was formed. The reaction mixture was stirred at room temperature for 1 hour. To the mixture was added a solution of toluidic acid hydrazide (16.23 mmol) in dry benzene (7.5 mL). The mixture was stirred at room temperature overnight. The mixture was filtered with Hyflo. The mixture was concentrated in a vacuum to give dimethyl (1-diazido-2-oxopropyl)phosphonate.

Dimethyl (1-Diazo-2-oxopropyl)phosphonate 준비 용품 및 원자재

원자재

준비 용품


Dimethyl (1-Diazo-2-oxopropyl)phosphonate 공급 업체

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