跳转至内容
Merck
所有图片(1)

主要文件

查看所有文档

D12600

Sigma-Aldrich

3,4-二氨基苯甲酸

97%

别名:

4-Carboxy-o-phenylenediamine

登录查看公司和协议定价
所有图片(1)

About This Item

线性分子式:
(H2N)2C6H3CO2H
CAS号:
619-05-6
分子量:
152.15
Beilstein:
775892
EC 号:
210-577-2
MDL编号:
MFCD00007726
UNSPSC代码:
12352200
PubChem化学物质编号:
24893391
NACRES:
NA.22

方案

97%

表单

powder

反应适用性

reaction type: solution phase peptide synthesis

mp

208-210 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

Nc1ccc(cc1N)C(O)=O

InChI

1S/C7H8N2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,8-9H2,(H,10,11)

InChI key

HEMGYNNCNNODNX-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

应用

3,4-二氨基苯甲酸可用于制备：
  • 席夫碱衍生物（通过与取代醛及其相应的金属络合物反应生成）
  • 聚（2，5-苯并咪唑）(ABPBI) 聚合物（通过与甲磺酸和P2O5反应生成）
  • 适用于H2O裂解反应的Pt基席夫碱络合物。

3,4-二氨基苯甲酸通过环缩合反应形成，如喹喔啉和 苯并咪唑。

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBG3445V
STBF8087V
STBF8807V
S39162
04328JJ

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。

搜索COA

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

N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(2), 376-383 (2007-12-28)
The Fourier Transform Raman and Fourier Transform infrared spectra of 3,4-diaminobenzoic acid (3,4-DABA) were recorded in the solid phase. Geometry optimizations were done without any constraint and harmonic-vibrational wave numbers and several thermodynamic parameters were calculated for the minimum energy
New platinum and ruthenium Schiff base complexes for water splitting reactions
Wang C, et al.
Dalton Transactions, 44(32), 14483-14493 (2015)
L A Cooper et al.
Antonie van Leeuwenhoek, 50(1), 53-62 (1984-01-01)
The effect of various compounds on growth, melanin biosynthesis and cell differentiation was studied in a hyaline (SH25) and a pigmented (SH25B) strain of Microdochium bolleyi. Dark pigment production by the hyaline strain was induced by the presence of DOPA
S Ram et al.
Journal of medicinal chemistry, 35(3), 539-547 (1992-02-07)
A series of methyl and ethyl 5-(alkoxycarbonyl)-1H-benzimidazole-2-carbamates (7-19) and methyl 5-carbamoyl-1H-benzimidazole-2-carbamates (24-34) have been synthesized via the reaction of an appropriate alcohol or amine with the acid chloride derivatives 6a or 6b at room temperature. Reaction of an alcohol with
New 3, 4-diaminobenzoic acid Schiff base compounds and their complexes: Synthesis, characterization and thermodynamics
Mohammadi K, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 122, 179-185 (2014)
查看所有相关文献

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.

联系客户支持