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Merck
모든 사진(1)

Key Documents

446882

Sigma-Aldrich

Perfluorohexyl bromide

98%

동의어(들):

1-Bromotridecafluorohexane

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About This Item

Linear Formula:
CF3(CF2)5Br
CAS Number:
Molecular Weight:
398.95
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

형태

liquid

refractive index

n20/D 1.3 (lit.)

bp

97 °C (lit.)

density

1.871 g/mL at 25 °C (lit.)

작용기

bromo
fluoro

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br

InChI

1S/C6BrF13/c7-5(16,17)3(12,13)1(8,9)2(10,11)4(14,15)6(18,19)20

InChI key

JTYRBFORUCBNHJ-UHFFFAOYSA-N

애플리케이션

Employed in the preparation of perfluorononanal by hydroformylation.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

Intra-abdominal sepsis and perfluorocarbons: mechanism of protection.
D B Hoyt et al.
Current surgery, 39(3), 165-167 (1982-05-01)
Douglass et al.
The Journal of organic chemistry, 65(5), 1434-1441 (2000-05-18)
A triphenylsilyl group is used as an auxiliary in the synthesis of heterodisubstituted p-carboranes via triphenylsilyl-p-carborane (1). The preparation of 1 is statistical, but with recovery of the starting p-carborane, the effective conversion to 1 is about 90%. Carborane 1
S L Wootton et al.
AJR. American journal of roentgenology, 161(2), 409-416 (1993-08-01)
The disadvantages of water-soluble gastrointestinal contrast agents include high osmolality, contrast dilution, and severe toxicity if aspirated. Perfluorocarbons are nontoxic in the lung and peritoneal cavity. Because perfluorocarbons are immiscible with water, they have no osmotic effect and cannot be
Zhang Feng et al.
Angewandte Chemie (International ed. in English), 54(4), 1270-1274 (2014-12-04)
An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction proceeds under mild reaction conditions with high efficiency and broad substrate scope, and provides a general and straightforward access
M Scrime et al.
Journal of pharmaceutical sciences, 70(11), 1199-1201 (1981-11-01)
Beagle dogs received single perfluorohexyl bromide doses, either 30.2 g/kg po or 3.8 g/kg intratracheally. The apparent first-order plasma half-life during the terminal elimination phase was approximately 8 hr after oral treatment and greater than 8 hr after intratracheal administration.

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