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(1S,2R)-(-)-cis-1-Amino-2-indanol (1S,2R)-(-)-顺式-1-氨基-2-茚醇

规格: 98%
CAS: 126456-43-7
产品编号: H84721
MDL: MFCD00216655
品牌: INFI
Chemical Name(1S,2R)-(-)-cis-1-Amino-2-indanol
Synonym (1S,2R)-(-)-1-Amino-2-hydroxyindan (1S,2R)-(-)-1-氨基-2-茚醇 (1S,2R)-(-)-顺式-1-氨基-2-茚醇 1-氨基-2-吲哚醇,(1S,2R)-(-)-氨基茚醇
MDL NumberMFCD00216655
Beilstein Registry Number4292559
CAS Number126456-43-7
PubChem Substance ID87563059
EC Number250-023-7
Reaxys-RN4292559
Chemical Name Translation(1S,2R)-(-)-顺式-1-氨基-2-茚醇
LabNetwork Molecule IDLN00215349
IUPAC Name(1S,2R)-1-amino-2,3-dihydro-1H-inden-2-ol
  • {PUB} ChEMBL|DrugBank|PubChem --- Design and Synthesis of a Series of (2R)-N4-Hydroxy-2-(3-hydroxybenzyl)-N- [(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden- 1-yl]butanediamide Derivatives as Potent, Selective, and Orally Bioavailable Aggrecanase Inhibitors --- https://pubmed.ncbi.nlm.nih.gov/11585439
  • {PUB} ChEMBL|PubChem|The Cambridge Structural Database --- Potent P1′ biphenylmethyl substituted aggrecanase inhibitors --- https://pubmed.ncbi.nlm.nih.gov/11738583
  • {PUB} PubChem --- Enantioselective Acylation of 1,2- and 1,3-Diols Catalyzed by Aminophosphinite Derivatives of (1S,2R)-1-Amino-2-indanol --- https://pubmed.ncbi.nlm.nih.gov/22260086
  • {PUB} PubChem --- Synthesis of enantiomerically pure trans‐(1R,2R)‐ and cis‐(1S,2R)‐1‐amino‐2‐indanol by lipase and ω‐transaminase --- https://pubmed.ncbi.nlm.nih.gov/16302257
  • {PUB} PubChem|Springer Nature --- Computational inhibitor design against malaria plasmepsins --- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11136018
  • {PUB} PubChem|Springer Nature --- Engineering an indene bioconversion process for the production of cis-aminoindanol: a model system for the production of chiral synthons --- https://pubmed.ncbi.nlm.nih.gov/12172601
  • {PUB} PubChem|Springer Nature --- The Petasis Reaction: Applications and Organic Synthesis—A Comprehensive Review --- https://pubmed.ncbi.nlm.nih.gov/39856385
  • {PUB} Springe
  • {PUB} Springer
  • {PUB} Springer Nature --- Asymmetric 1,3-Dipolar Cycloaddition Reactions Catalyzed by Heterocycle-Based Metal Complexes --- https://doi.org/10.1007/7081_2009_1
  • {PUB} Springer Nature --- Family I.3 lipase: bacterial lipases secreted by the type I secretion system --- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11136109
  • {PUB} Springer Nature --- From Racemates to Single Enantiomers – Chiral Synthetic Drugs over the last\\n20 Years --- https://pubmed.ncbi.nlm.nih.gov/23605355
  • {PUB} Springer Nature --- Metabolic Engineering of Indene Bioconversion in Rhodococcus sp. --- https://doi.org/10.1007/3-540-45300-8_5
  • 126456-43-7 H84721 (1S,2R)-(-)-cis-1-Amino-2-indanol	(1S,2R)-(-)-顺式-1-氨基-2-茚醇

    化学属性

    Mol. FormulaC9H11NO
    Mol. Weight149.19
    Melting Point118-121
    Density1.212
    TSCANo
    Stability对空气敏感
    Appearance white to off-white pwdr.

    *以上化合物性质及应用等信息仅供参考