ジクロロイソプロピルホスフィンオキシド

Isopropylphosphonic dichloride

HCID 2793751CAS 1498-46-0

部分構造検索類似構造を探す

基本情報

標準SMILES: CC(C)P(=O)(Cl)Cl
InChIKey: KLHAQQISVPLKAI-UHFFFAOYSA-N
分子式: C3H7Cl2OP
平均分子量: 160.96 g/mol
単同位体質量: 159.9611572

名称と識別子

優先名称: Isopropylphosphonic dichloride
IUPAC: 2-dichlorophosphorylpropane
現地名: ジクロロイソプロピルホスフィンオキシド
英語名: Isopropyl phosphonic dichloride
分子式: C3H7Cl2OP
分子量: 160.97

名称と別名

1498-46-0Isopropylphosphonic dichloride2-dichlorophosphorylpropaneISOPROPYL PHOSPHONIC DICHLORIDEPhosphonic dichloride, (1-methylethyl)-SCHEMBL2020126Propan-2-ylphosphonic dichlorideDTXSID10383154AKOS022186306DB-009755ジクロロイソプロピルホスフィンオキシドAURORA KA-6763

名称をさらに表示

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

データベース識別子

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

物性

構造計算による物性

XLogP: 1.7
極性表面積: 17.1 Å²
水素結合供与体数: 0
水素結合受容体数: 1
回転可能結合数: 1
重原子数: 7
形式電荷: 0
複雑度: 95

物理化学的性質

沸点: 71.5 · 71.5-72.5 °C(Press: 11 Torr)
比重(密度): 1.2979 g/cm3 · 1.2979 g/cm3
溶解性: エチレングリコールおよびジエチルエーテルと混和します。

安全と法規制

GHS分類

GHS Classification · 5 件

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.

安全データ

ridadr: UN3265
hazard_class: 8
packing_group: II

化学と産業

応用分野

使用Isopropylphosphonic 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.