메틸 포스폰 디염화물
메틸포스포닉다이클로라이드 · 메틸포스폰디염화물 · 메틸포스폰이염화물 · 메틸 포스포닉 다이클로라이드 · Methylphosphonyl dichloride · NA 9206 · CH3POCl2 · methylpho

식별자 및 물리적 특성
| CAS No. | 676-97-1 |
|---|---|
| 분자식 | CH3Cl2OP |
| 평균 분자량 | 132.91 g/mol |
| 단동위원소 질량 | 131.92985671 g/mol |
| SMILES | CP(=O)(Cl)Cl |
| InChIKey | SCLFRABIDYGTAZ-UHFFFAOYSA-N |
| PubChem CID | 12671 |
| EC No. | 211-634-4 |
| DTXSID | DTXSID6060979 |
| 현지명 | 메틸 포스폰 디염화물 |
화학 및 물리적 성질
| XLogP | 1 |
|---|---|
| 극성 표면적 | 17.1 |
| 수소 결합 공여자 수 | 0 |
| 수소 결합 수용자 수 | 1 |
| 회전 가능 결합 수 | 0 |
| 무거운 원자 수 | 5 |
| 형식 전하 | 0 |
| 복잡도 | 64 |
| 물질 분류 | Toxic Gases & Vapors -> Acid Halides |
| SpringerMaterials Properties | Schoenflies notation |
| 냄새 | Pungent odor |
| 밀도 | 1.39 g/cu cm at 38 °C1.468 g/mL at 25 °C(lit.) |
| Color/Form | Low melting solid |
| 끓는 점 | 325 °F162 °C162 °C @760 [mm Hg]163 °C(lit.) |
| Decomposition | When heated to decomposition it emits toxic fumes of /hydrogen chloride and phosphorus oxides/. |
| 녹는점 | 95-99 °F32 °C31-34 °C |
| 증기압 | 760 mm Hg at 163 °C760 mm Hg ( 163 °C) |
| 굴절률 | Index of refraction: 1.462 at 38 °C |
| Physical Description | Strongly irritates skin. Contact may destroy or irreversibly alter skin tissue. Very toxic by ingestion, inhalation, or by skin absorption. Combustible, though may be difficult to ignite.A solid below 95-99 deg F[HSDB] Colorless liquidMelting point = 90-93 deg F[MSDSonline] |
| Other Experimental Properties | Easily hydrolyzed |
| 인화점 | >110°C |
| 용해도 | 아세토니트릴(약간 용해됨), 클로로포름 |
| 물리적 상태 | 고체 |
| 용해도 | 물에 용해됩니다. |
| BRN | 1071305 |
| 안정성 | 안정적이지만 물이나 습기가 있으면 분해될 수 있습니다. 물, 강염기, 강산화제와 호환되지 않습니다. |
| EPA | Methylphosphonic dichloride (676-97-1) |
화학적 성질
Methyl phosphonic dichloride is a low melting solid or colorless to pale yellow liquid. Pungent odor.
안전 및 규제
| GHS 분류 | DangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P271, P280, P284, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P320, P321, P363, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 43 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.H314: Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
|---|---|
| Hazards Identification | Toxic/poison by inhalation (TIH/PIH) |
| 규제 정보 | Chemical: Phosphonic dichloride, methyl-The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| 운송 라벨(DOT) | Poison Inhalation Hazard Corrosive |
| 화재 위험 | This material may burn but does not ignite readily. May ignite other combustible materials (wood, paper, oil, etc.). Reacts violently with water. Flammable poisonous gases may accumulate in tanks and hopper cars. Runoff to sewer may create fire or explosion hazard. Contact causes severe burns to skin and eyes. Runoff from fire control or dilution water may cause pollution. Violent reaction with water. (EPA, 1998)· EXCEPT FOR ACETIC ANHYDRIDE (UN1715), THAT IS FLAMMABLE, some of these materials may burn, but none ignite readily. |
| 화재 가능성 | It may be combustible though it may require some effort to ignite. |
| 건강 유해성 | Poisonous if inhaled or swallowed. Contact causes severe burns to skin and eyes. (EPA, 1998)· CORROSIVE and/or TOXICinhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. |
| 유해성 요약 | Reacts with water to generate hydrogen chlorideContact with substance causes severe burns[CAMEO] Causes burnsVery toxic by inhalation--may cause chemical pneumonitis[MSDSonline] |
| 운송 번호 및 가이드(DOT) | 9206 137 |
용도
용도
suzuki reaction
일반 설명
Strongly irritates skin. Contact may destroy or irreversibly alter skin tissue. Very toxic by ingestion, inhalation, or by skin absorption. Combustible, though may be difficult to ignite.
제조 및 합성 방법
생산 방법
The oxidation of lowvalency organophosphorus compounds is important mainly in the case of the thiophosphonic acid chlorides. This method is used in the production of methylphosphonic acid dichloride by reaction of methyldichlorophosphine with sulfuryl chloride or chlorosulfuric acid. Elemental sulfur reacts with MePCl2 in the presence of catalytic quantities of tetraalkylphosphonium salts to form methylthiophosphonic acid dichloride.