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About This Item
经验公式（希尔记法）:
C11H10O2
CAS号:
分子量:
174.20
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
98%
表单
powder
mp
201-203 °C (lit.)
SMILES字符串
CC1=C(Cc2ccccc12)C(O)=O
InChI
1S/C11H10O2/c1-7-9-5-3-2-4-8(9)6-10(7)11(12)13/h2-5H,6H2,1H3,(H,12,13)
InChI key
RONBYWGSEXDEKC-UHFFFAOYSA-N
一般描述
3-Methylindene-2-carboxylic acid undergoes asymmetric hydrogenation over Pd/Al2O3 in the presence of cinchonidine as a chiral modifier.
应用
3-Methylindene-2-carboxylic acid was used in the synthesis of:
- LKS01-B650, an imaging probe that selectively binds the catalytically active LMP7 subunit of immunoproteasome in living cells
- 1-methylindane-2-carboxylic acid via reduction with sodium amalgam
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
cis-and trans-2-Substituted 1-methylindanes.
Shadbolt, RS.
J. Chem. Soc. Sect. C, 7, 920-922 (1970)
Lalit Kumar Sharma et al.
Chembiochem : a European journal of chemical biology, 13(13), 1899-1903 (2012-07-19)
Probing the unknown: The immunoproteasome, an alternative form of the constitutive proteasome, has been implicated in a number of pathological states such as cancer and autoimmune diseases. In an effort to understand the role of the immunoproteasome in cells, the
Asymmetric hydrogenation of indene carboxylic acids: stereochemistry of hydrogen addition.
Borszeky K, et al.
Tetrahedron Asymmetry, 10(24), 4781-4789 (1999)
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