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2,3-Diaminobenzoic acid

95%

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About This Item

Fórmula empírica (Notação de Hill):
C7H8N2O2
Peso molecular:
152.15
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:

Ensaio

95%

pf

198-204 °C

aplicação(ões)

peptide synthesis

cadeia de caracteres SMILES

Nc1cccc(C(O)=O)c1N

InChI

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

chave InChI

KKTUQAYCCLMNOA-UHFFFAOYSA-N

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Classificações de perigo

Acute Tox. 4 Oral - Eye Irrit. 2

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Geun Woo Dong et al.
Clinical and experimental otorhinolaryngology, 2(1), 13-19 (2009-05-13)
Despite the ongoing development of treatment protocols for laryngeal squamous cell carcinoma (LSCC), the patients suffering with this malady have shown only a modestly improved outcome. This poor outcome has been attributed to the lack of therapy that's individualized to
Takeshi Matsumoto et al.
Scientific reports, 8(1), 14623-14623 (2018-10-04)
We report the photochemical carboxylation of o-phenylenedimamine in the absence of a base and an electron donor under an atmosphere of CO2, which afforded 2,3-diaminobenzoic acid (DBA) in 28% synthetic yield and 0.22% quantum yield (Φ(%)). The synthetic yield of
Anal Jana et al.
Journal of photochemistry and photobiology. B, Biology, 214, 112091-112091 (2020-12-08)
Formaldehyde (FA), a simple reactive carbonyl molecule, is endogenously produced in the cell at various physiological condition. At elevated level, FA causes severe cell toxicity as well as damage in macromolecules such proteins and DNA. For detecting FA in living
Bettina S Buchmaier et al.
PloS one, 8(7), e68301-e68301 (2013-07-23)
Osmotic stress has been shown to regulate cytoskeletal protein expression. It is generally known that vimentin is rapidly degraded during apoptosis by multiple caspases, resulting in diverse vimentin fragments. Despite the existence of the known apoptotic vimentin fragments, we demonstrated
Alexander von Tesmar et al.
Cell chemical biology, 24(10), 1216-1227 (2017-09-12)
In vitro reconstitution and biochemical analysis of natural product biosynthetic pathways remains a challenging endeavor, especially if megaenzymes of the nonribosomal peptide synthetase (NRPS) type are involved. In theory, all biosynthetic steps may be deciphered using mass spectrometry (MS)-based analyses of

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