추천 제품
분석
98%
형태
powder
mp
201-203 °C (lit.)
SMILES string
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
일반 설명
3-Methylindene-2-carboxylic acid undergoes asymmetric hydrogenation over Pd/Al2O3 in the presence of cinchonidine as a chiral modifier.
애플리케이션
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
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
cis-and trans-2-Substituted 1-methylindanes.
J. Chem. Soc. Sect. C, 7, 920-922 (1970)
Asymmetric hydrogenation of indene carboxylic acids: stereochemistry of hydrogen addition.
Tetrahedron Asymmetry, 10(24), 4781-4789 (1999)
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
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