跳转至内容
Merck

232793

Sigma-Aldrich

3-甲酰苯甲酸

97%

别名:

3-羧基苯甲醛, 异酞醛酸

登录查看公司和协议定价


About This Item

线性分子式:
HO2CC6H4CHO
CAS号:
分子量:
150.13
Beilstein:
2206413
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

powder

mp

173-175 °C (lit.)

溶解度

methanol: soluble 100 mg/mL, clear to slightly hazy, colorless to very faintly brown(lit.)

官能基

aldehyde
carboxylic acid

SMILES 字串

[H]C(=O)c1cccc(c1)C(O)=O

InChI

1S/C8H6O3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-5H,(H,10,11)

InChI 密鑰

UHDNUPHSDMOGCR-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般說明

3-甲酰苯甲酸是一种极性芳香醛,常用于还原合成3-羟甲基苯甲酸。

應用

3-甲酰基苯甲酸已被用于合成:
  • 通过Ugi 4中心3组分反应的双环顺式-2-氮杂环丁酮衍生物合成
  • 带有会聚羟基的甾族超结构封端的卟啉
  • 3-[(4-氨基-1,2-二氢-1-氧代-2-苯基-1,2,4-三唑[4,3-a]喹喔啉-6-基)氨基]甲基苯甲酸

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

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

dust mask type N95 (US), Eyeshields, Gloves


从最新的版本中选择一种:

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

Synthesis of Alicyclic-lactams via the Ugi Reaction on a Solid Support.
Gedey S, et al.
Letters in Organic Chemistry, 1(3), 215-220 (2004)
Suhman Chung et al.
Nature chemical biology, 5(6), 407-413 (2009-04-28)
The linking together of molecular fragments that bind to adjacent sites on an enzyme can lead to high-affinity inhibitors. Ideally, this strategy would use linkers that do not perturb the optimal binding geometries of the fragments and do not have
Vittoria Colotta et al.
Bioorganic & medicinal chemistry, 11(24), 5509-5518 (2003-12-04)
In previous papers (Colotta, V. et al. Arch. Pharm. Pharm. Med. Chem. 1999, 332, 39. Colotta, V. et al. J. Med. Chem. 2000, 43, 1158) we reported the synthesis and binding affinity at bovine (b) A(1) and A(2A) and human
Synthesis, binding properties and self-functionalization of a steroid-capped porphyrin.
Richard P and Jeremy KM.
Journal of the Chemical Society. Chemical Communications, 8, 574-577 (1991)
Steven R Inglis et al.
Journal of medicinal chemistry, 52(19), 6097-6106 (2009-09-08)
Penicillin binding proteins (PBPs) catalyze steps in the biosynthesis of bacterial cell walls and are the targets for the beta-lactam antibiotics. Non-beta-lactam based antibiotics that target PBPs are of interest because bacteria have evolved resistance to the beta-lactam antibiotics. Boronic

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门