登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式(希尔记法):
C19H13ClO
化学文摘社编号:
分子量:
292.76
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
255-857-5
Beilstein/REAXYS Number:
237712
MDL number:
Assay:
97%
Form:
solid
InChI key
HTGMODSTGYKJDG-UHFFFAOYSA-N
InChI
1S/C19H13ClO/c20-19(14-8-2-1-3-9-14)15-10-4-6-12-17(15)21-18-13-7-5-11-16(18)19/h1-13H
SMILES string
ClC2(c1ccccc1)c3ccccc3Oc4ccccc24
assay
97%
form
solid
solubility
chloroform: soluble 25 mg/mL, clear, yellow to orange
Application
9-Chloro-9-phenylxanthene was used in the preparation of (1S,5S,6R,8S)-6-[(allyloxycarbonyl)oxy]-5-(trifluoroacetamido)-8-[9′-(9′-phenylxanthenyl)oxy]-2-oxabicyclo(3.2.1)octane.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
I Pompizi et al.
Nucleic acids research, 28(14), 2702-2708 (2000-07-25)
The synthesis and incorporation into oligodeoxy-nucleotides of two novel, conformationally restricted abasic (AB) site analogs are described. The stability of oligonucleotide 18mer duplexes containing one such AB site opposite any of the four natural DNA bases was investigated by UV
The pixyl (Px) group: a novel photocleavable protecting group for primary alcohols.
Misetic A and Boyd MK.
Tetrahedron Letters, 39(13), 1653-1656 (1998)
The 9-phenylxanthen-9-yl protecting group.
Chattopadhyaya JB and Reese CB.
Journal of the Chemical Society. Chemical Communications, 15, 639-640 (1978)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持