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Merck
CN

130613

5-溴藜芦醛

98%

别名:

3-溴-4,5-二甲氧基苯甲醛

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关于此项目

线性分子式:
BrC6H2(OCH3)2CHO
化学文摘社编号:
分子量:
245.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-113-2
MDL number:
Assay:
98%
Form:
powder
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Quality Level

assay

98%

form

powder

mp

63-64 °C (lit.)

functional group

aldehyde, bromo

SMILES string

COc1cc(C=O)cc(Br)c1OC

InChI

1S/C9H9BrO3/c1-12-8-4-6(5-11)3-7(10)9(8)13-2/h3-5H,1-2H3

InChI key

ICVODPFGWCUVJC-UHFFFAOYSA-N

Application

5-Bromoveratraldehyde (3-Bromo-4,5-dimethoxybenzaldehyde) was used to prepare 1-phenyl-2-(4-aryl-1,3,4,5-tetrahydropyrido[2,3-b][1,4]diazepin-2-ylidene)-ethanones.


pictograms

Exclamation mark

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

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H Liszkiewicz et al.
Die Pharmazie, 61(6), 517-521 (2006-07-11)
A two-step, general synthesis of 1-phenyl-2-(4-aryl-1,3,4,5-tetrahydropyrido[2,3-b][1,4]diazepin-2-ylidene)-ethanones 3-9 is presented. This synthesis employs a condensation of 2,3-diaminopyridine with benzoylacetone followed by a basic-activated cyclization reaction with substituted benzaldehydes for final closure of the seven-membered ring. Molecular diversity is fixed by appropriate



全球贸易项目编号

货号GTIN
W215311-1KG-K04065265643191
W215355-1KG-K04065265648844
W215355-SAMPLE-K04065265648868
W215355-100G-K04065265648837
W215311-SAMPLE-K04065265643214
W215311-100G-K04065265643184
B4383-100ML04061838177582
130613-5G04061831818482