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经验公式(希尔记法):
C9H10O2
化学文摘社编号:
分子量:
150.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
≥97.0% (sum of enantiomers, GC)
InChI
1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2/t9-/m0/s1
SMILES string
C1O[C@H]1COc2ccccc2
InChI key
FQYUMYWMJTYZTK-VIFPVBQESA-N
assay
≥97.0% (sum of enantiomers, GC)
Application
Reactant involved in the synthesis of:
Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase
- Neuroprotective small molecules
- Piperidinol analogs for studies of anti-tuberculosis activity
- 2-Substituted 3,4-dihydro-2H-1,4-benzoxazines via cyclization of hydroxyl sulfonamides
- Bicyclic azetidines via ring opening, esterification, chlorination and intramolecular alkylation
- Bromoalkanes via ring opening and addition across C-O bonds
Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Carc. 1B - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
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