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149861

呋喃甲酰氯

Name: 呋喃甲酰氯
Brand: ALDRICH

95%

别名:

2-呋喃碳酰氯

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关于此项目

经验公式（希尔记法）:

C₅H₃ClO₂

化学文摘社编号:

527-69-5

分子量:

130.53

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848981

EC Number:

208-422-9

Beilstein/REAXYS Number:

110144

MDL number:

MFCD00003228

Assay:

95%

Form:

liquid

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属性

Quality Level

200

assay

95%

form

liquid

refractive index

n20/D 1.531 (lit.)

bp

173-174 °C (lit.)

mp

−2 °C (lit.)

density

1.324 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

ClC(=O)c1ccco1

InChI

1S/C5H3ClO2/c6-5(7)4-2-1-3-8-4/h1-3H

InChI key

OFTKFKYVSBNYEC-UHFFFAOYSA-N

说明

Application

2-呋喃甲酰氯用于聚乙氧基化醇及其硫酸盐混合物的反应。它也用于制备 S-2-呋喃甲酰-O-烷基二硫代碳酸酐。

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302 + H312 + H332,H314

pcodes

P261 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

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

法规信息

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Characterisation of ethoxylated fatty chains of anionic surfactants and determination of residual ethoxylated fatty alcohols.

Julien Morvan et al.

Analytical and bioanalytical chemistry, 384(6), 1409-1415 (2006-02-28)

Bachus et al. [1] recently described a new derivatisation method using 2-furoyl chloride for the characterisation of mixtures of polyethoxylated alcohols and their corresponding sulfates. This paper deals with the control of the derivatisation steps; hydrolysis and extraction conditions were

Synthesis and radiosensitizing properties of some 2-furancarboxylic acid derivatives.

J Tułecki et al.

Polish journal of pharmacology and pharmacy, 37(5), 709-715 (1985-09-01)

New S-2-furoyl-O-alkyldithiocarbonic anhydrides have been obtained by condensation of 2-furoyl chloride with potassium O-alkyl-dithiocarbonates. The toxicity and radiosensitizing activity of these compounds were determined.

Therapeutic potential of selanyl amide derivatives in the in vitro anticholinesterase activity and in in vivo antiamnesic action.

Ethel A Wilhelm et al.

Canadian journal of physiology and pharmacology, 98(5), 304-313 (2019-12-11)

The present study evaluated the in vitro acetylcholinesterase (AChE) inhibitor activity of two new selanyl amide derivatives in cerebral structures of mice. Our results demonstrated that N-(2-(3-(phenylselanyl)propoxy)phenyl)furan-2-carboxamide (1) and N-(2-(3-(phenylselanyl)propoxy)phenyl)thiophene-2-carboxamide (2) inhibited the in vitro AChE activity in mice. Another

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全球贸易项目编号

货号	GTIN
149861-25G	04061838738509
149861-100G	04061838738493