跳转至内容
Merck
CN

535079

溴代丙二醛

97%

别名:

Bromomalondialdehyde

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:
BrCH(CHO)2
化学文摘社编号:
分子量:
150.96
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


Quality Level

assay

97%

mp

132-136 °C (lit.)

functional group

aldehyde, bromo

SMILES string

[H]C(=O)C(Br)C([H])=O

InChI

1S/C3H3BrO2/c4-3(1-5)2-6/h1-3H

InChI key

SURMYNZXHKLDFO-UHFFFAOYSA-N

Application

用于构建 1,4-二氢喹啉,其 C-3 手性亚砜基可作为环状 NADH 模型,参与苯甲酰甲酸甲酯的不对称还原反应,生成苯乙醇酸甲酯。
用于由取代基鸟嘌呤形成乙二醛衍生加合物


pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



Synlett, 441-441 (2005)
E C Taylor et al.
Investigational new drugs, 14(3), 281-285 (1996-01-01)
A new and extremely efficient synthesis of DDATHF from 4-vinylbenzoic acid and bromomalondialdehyde as precursors has been developed which proceeds in 48% overall yield.
Anne-Mari Ruohola et al.
Organic & biomolecular chemistry, 2(13), 1943-1950 (2004-07-01)
Reactions of 9-ethylguanine, 2'-deoxyguanosine and guanosine with bromomalondialdehyde in aqueous buffers over a wide pH-range were studied. The main products were isolated and characterized by (1)H and (13)C NMR and mass spectroscopy. The final products formed under acidic and basic



全球贸易项目编号

货号GTIN
535079-25G04061831820881
535079-5G04061831811131