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Merck
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主要文件

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515604

Sigma-Aldrich

4-碘溴苄

95%

别名:

α-Bromo-4-iodotoluene, 1-(Bromomethyl)-4-iodobenzene, 4-(Bromomethyl)iodobenzene

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About This Item

线性分子式:
IC6H4CH2Br
CAS号:
16004-15-2
分子量:
296.93
Beilstein:
2325160
MDL號碼:
MFCD00209656
分類程式碼代碼:
12352100
PubChem物質ID:
24873836
酶委員會索引編號:
7000468
NACRES:
NA.22

品質等級

100

化驗

95%

mp

78-82 °C (lit.)

官能基

bromo
iodo

儲存溫度

2-8°C

SMILES 字串

BrCc1ccc(I)cc1

InChI

1S/C7H6BrI/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2

InChI 密鑰

BQTRMYJYYNQQGK-UHFFFAOYSA-N

相关类别

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H314

危險分類

Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKBX9626V
MKBX4313V
MKBW8625V
MKBW5516V
MKBN8942V

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Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 142-142 (2015)
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 537-537 (2014)
M E Van Dort et al.
Bioorganic & medicinal chemistry letters, 11(8), 1045-1047 (2001-05-01)
A series of arylhydantoin derivatives modeled after the antiandrogen RU 58841 was generated to identify potential candidates for development as androgen receptor (AR) radioligands. Side-chain modified derivatives of RU 58841, suitable for labeling with either carbon-11 or radiohalogens (fluorine-18, iodine-123)
S De Bruyne et al.
Journal of labelled compounds & radiopharmaceuticals, 52(8), 304-311 (2009-09-12)
Dopamine transporter (DAT) neuroimaging is a useful tool in Parkinson's disease diagnosis, staging and follow-up providing information on the integrity of the dopaminergic neurotransmitter system in vivo. 4-(2-(Bis(4-fluorophenyl)-methoxy)ethyl)-1-(4-iodobenzyl)piperidine (7) has nanomolar affinity for DAT and better selectivity over the other
Guillermo E Negrón-Silva et al.
Molecules (Basel, Switzerland), 18(4), 4613-4627 (2013-04-20)
Ten 1,4-disubstituted 1,2,3-triazoles were synthesized from one of 1-(azido-methyl)benzene, 1-(azidomethyl)-4-fluorobenzene, 1-(azidomethyl)-4-chlorobenzene, 1-(azidomethyl)-4-bromobenzene or 1-(azidomethyl)-4-iodobenzene, generated in situ from sodium azide and the corresponding benzyl halide, and dipropargyl uracil or dipropargyl thymine. Optimal experimental conditions were established for the conventional click
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