主要文件

查看所有文档

24-2830

三氯化磷

Name: 三氯化磷
Brand: SAJ

CP

别名:

氯化磷(III)

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

PCl₃

化学文摘社编号:

7719-12-2

分子量:

137.33

EC Number:

231-749-3

UNSPSC Code:

12352300

PubChem Substance ID:

329752622

Beilstein/REAXYS Number:

969177

MDL number:

MFCD00011438

Grade:

Bp:

74-78 °C (lit.)

Vapor pressure:

100 mmHg ( 20 °C), 125 mmHg ( 25 °C), 385 mmHg ( 55 °C)

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

grade

vapor density

4.75 (vs air)

vapor pressure

100 mmHg ( 20 °C), 125 mmHg ( 25 °C), 385 mmHg ( 55 °C)

form

liquid

availability

available only in Japan

dilution

(for analytical testing)

refractive index

n20/D 1.5148 (lit.)

bp

74-78 °C (lit.)

mp

−112 °C (lit.)

density

1.574 g/mL at 20 °C (lit.)

SMILES string

ClP(Cl)Cl

InChI

1S/Cl3P/c1-4(2)3

InChI key

FAIAAWCVCHQXDN-UHFFFAOYSA-N

说明

Still not finding the right product?

Explore all of our products under 三氯化磷

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT RE 2 Inhalation

target_organs

Respiratory Tract

supp_hazards

EUH014,EUH029

存储类别

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

新产品

此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助，请联系客户支持

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

First synthesis of etidronate partial amides starting from PCl3.

Petri A Turhanen et al.

Organic & biomolecular chemistry, 1(18), 3223-3226 (2003-10-07)

Methods for the preparation of mixed tetra-amide esters 1 and 2, the partial amide ester 3, and tri- and P,P-diamides 4 and 5 from monophosphorus spieces 12, 8 and 9, respectively, were developed. Compounds 8 and 9 were obtained from

Phosphorus trichloride-mediated and microwave-assisted synthesis of a small collection of amides bearing strong electron-withdrawing group substituted anilines.

Matteo Colombo et al.

Journal of combinatorial chemistry, 11(3), 335-337 (2009-03-31)

A diversity oriented, microwave assisted synthesis of N-substituted 2-hydro-4-amino-pyrido[2,3-d]pyrimidin-7(8H)-ones.

Núria Mont et al.

Molecular diversity, 13(1), 39-45 (2008-11-28)

A protocol for the synthesis of N-substituted 2-hydro-4-amino-pyrido[2,3-d]pyrimidin-7(8H)-ones (11) is described. Thus, the formylation of a 2-aminopyridone 12 in 85% formic acid/Ac(2)O, proceeding via in situ cyclization to the intermediate formamide 13, affords the corresponding 2-hydro-4-oxo-pyridopyrimidine 14, which is converted

查看所有相关文献