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推薦產品
等級
technical grade
化驗
90%
形狀
liquid
光學活性
[α]20/D −19°, c = 1 in acetone
折射率
n20/D 1.511 (lit.)
bp
105-109 °C/0.1 mmHg (lit.)
密度
1.12 g/mL at 25 °C (lit.)
官能基
ester
hydroxyl
phenyl
SMILES 字串
C[C@H](O)C(=O)OCc1ccccc1
InChI
1S/C10H12O3/c1-8(11)10(12)13-7-9-5-3-2-4-6-9/h2-6,8,11H,7H2,1H3/t8-/m0/s1
InChI 密鑰
ZYTLPUIDJRKAAM-QMMMGPOBSA-N
一般說明
Benzyl (S)-(-)-lactate may be used in the preparation of (R)-(+)-methyl 7-(1-(benzyloxy)-1-oxopropan-2-yloxy)-2-oxo-2H-chromene-3-carboxylate.[1]
儲存類別代碼
10 - Combustible liquids
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
Synthesis and evaluation of two coumarin-type derivatization reagents for fluorescence detection of chiral amines and chiral carboxylic acids.
Mertens MD and Gutschow M.
Chirality, 25(12), 957-964 (2013)
Bunta Watanabe et al.
PloS one, 10(8), e0136242-e0136242 (2015-08-22)
CCG-1423 suppresses several pathological processes including cancer cell migration, tissue fibrosis, and the development of atherosclerotic lesions. These suppressions are caused by inhibition of myocardin-related transcription factor A (MRTF-A), which is a critical factor for epithelial-mesenchymal transition (EMT). CCG-1423 can
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