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Merck
CN

515396

3,5-二溴苯甲醛

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关于此项目

线性分子式:
Br2C6H3CHO
化学文摘社编号:
分子量:
263.91
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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mp

84-88 °C (lit.)

Quality Segment

functional group

aldehyde, bromo

SMILES string

Brc1cc(Br)cc(C=O)c1

InChI

1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H

InChI key

ZLDMZIXUGCGKMB-UHFFFAOYSA-N

Application

Reactant involved in:
  • Suzuki-Miyaura cross-coupling reactions
  • Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
  • Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
  • Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
  • Allylic alkylation
  • Synthesis of C2-symmetric biphosphine ligand I


pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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相关内容


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Double-action haloketones: A super silyl group enabled the first highly diastereoselective Mukaiyama aldol reactions of α-chloro- and α-fluoroketones with a wide range of aldehydes, providing anti-β-siloxy-α-haloketones. This process is compatible with one-pot double-aldol methodology and allows for rapid access to
Conformational Behavior of Conjugated Polymers With Oligo (phenylene vinylene) Side Chains.
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全球贸易项目编号

货号GTIN
515396-5G04061832493336