이소프로필포스포닉디클로라이드

Isopropylphosphonic dichloride

HCID 2793751CAS 1498-46-0

부분 구조 검색 유사 구조 찾기

기본 정보

표준 SMILES: CC(C)P(=O)(Cl)Cl
InChIKey: KLHAQQISVPLKAI-UHFFFAOYSA-N
분자식: C3H7Cl2OP
평균 분자량: 160.96 g/mol
단동위원소 질량: 159.9611572

이름 및 식별자

우선 이름: Isopropylphosphonic dichloride
IUPAC: 2-dichlorophosphorylpropane
현지명: 이소프로필포스포닉디클로라이드
영어명: Isopropyl phosphonic dichloride
분자식: C3H7Cl2OP
분자량: 160.97

이름 및 동의어

1498-46-0Isopropylphosphonic dichloride2-dichlorophosphorylpropaneISOPROPYL PHOSPHONIC DICHLORIDEPhosphonic dichloride, (1-methylethyl)-SCHEMBL2020126Propan-2-ylphosphonic dichlorideDTXSID10383154AKOS022186306DB-009755이소프로필포스포닉디클로라이드AURORA KA-6763

이름 더 보기

1-METHYLETHYL-PHOSPHONICDICHLORIDEP-(1-Methylethyl)phosphonic dichloridePhosphonic dichloride, P-(1-methylethyl)-Isopropylphosphonic dichloride, tech. 90%

데이터베이스 식별자

CAS: 1498-46-0
PubChem CID: 2793751
DTXSID: DTXSID10383154
EC Number: 679-087-8
Nikkaji: J2.892.768A

물성

구조 계산 물성

XLogP: 1.7
극성 표면적: 17.1 Å²
수소 결합 공여자 수: 0
수소 결합 수용자 수: 1
회전 가능 결합 수: 1
무거운 원자 수: 7
형식 전하: 0
복잡도: 95

물리화학적 성질

끓는 점: 71.5 · 71.5-72.5 °C(Press: 11 Torr)
밀도: 1.2979 g/cm3 · 1.2979 g/cm3
용해도: 에틸렌 글리콜 및 디에틸 에테르와 혼합 가능.

안전 및 규제

GHS 분류

GHS Classification · 5건

Danger

H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 4 reports by companies from 1 notifications to the ECHA C&L Inventory.；Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

안전 데이터

ridadr: UN3265
포장분류: II
위험 등급: 8

화학 및 산업

응용 분야

용도Isopropylphosphonic dichloride is used as a raw material for the preparation of bis(fluoroalkyl) alkylphosphonates by reacting with fluoroalcohols in the presence of triethylamine as catalyst.