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About This Item
經驗公式（希爾表示法）:
C13H14N2O3
CAS號碼:
分子量：:
246.26
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.22
推薦產品
品質等級
化驗
98%
形狀
solid
光學活性
[α]24/D −21°, c = 1 in methanol
反應適用性
reaction type: solution phase peptide synthesis
mp
138-140 °C (lit.)
應用
peptide synthesis
SMILES 字串
C[C@H](NC(=O)Cc1c[nH]c2ccccc12)C(O)=O
InChI
1S/C13H14N2O3/c1-8(13(17)18)15-12(16)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7-8,14H,6H2,1H3,(H,15,16)(H,17,18)/t8-/m0/s1
InChI 密鑰
FBDCJLXTUCMFLF-QMMMGPOBSA-N
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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
Eyeshields, Gloves, type N95 (US)
Miguel A Uc-Chuc et al.
International journal of molecular sciences, 21(13) (2020-07-09)
Despite the existence of considerable research on somatic embryogenesis (SE), the molecular mechanism that regulates the biosynthesis of auxins during the SE induction process remains unknown. Indole-3-acetic acid (IAA) is an auxin that is synthesized in plants through five pathways.
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and
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