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594261

5-溴异喹啉

98%

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关于此项目

经验公式（希尔记法）:
C9H6BrN
化学文摘社编号:
34784-04-8
分子量:
208.05
NACRES:
NA.22
PubChem Substance ID:
24881493
UNSPSC Code:
12352100
MDL number:
MFCD01646405
Assay:
98%
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assay

98%

mp

83-87 °C (lit.)

functional group

bromo

SMILES string

Brc1cccc2cnccc12

InChI

1S/C9H6BrN/c10-9-3-1-2-7-6-11-5-4-8(7)9/h1-6H

InChI key

CYJZJGYYTFQQBY-UHFFFAOYSA-N

Application

用于钯催化的氨甲基化和胺化反应的原料。

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BGBB3053V
BGBB3053
MKAA1582
00414EJ
00409EH

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Gary A Molander et al.
Organic letters, 9(8), 1597-1600 (2007-03-21)
[reaction: see text] The Suzuki-Miyaura cross-coupling reaction of N,N-dialkylaminomethyltrifluoroborates with aryl halides allows the construction of an aminomethyl aryl linkage through a disconnection based on dissonant reactivity patterns. A variety of these aminomethyltrifluoroborate substrates were prepared in good to excellent
Qilong Shen et al.
Journal of the American Chemical Society, 128(31), 10028-10029 (2006-08-03)
A mild, palladium-catalyzed coupling of aryl halides with ammonia or lithium amide to form primary arylamines as the major product is described. These reactions occurred with excellent selectivity for formation of the primary arylamine over formation of the diarylamine (9.5:1

全球贸易项目编号

货号GTIN
594261-1G04061832643885
594261-5G04061832643892