380687
N,N-双[2-(对甲苯磺酰氧基)乙基]-对甲苯磺酰胺
97%
别名:
N,N-双[2-(甲苯磺酰氧基)乙基]-对甲苯磺酰胺, N,O,O′-三甲苯磺酰二乙醇胺
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选择尺寸
关于此项目
线性分子式:
CH3C6H4SO2N(CH2CH2OSO2C6H4CH3)2
化学文摘社编号:
分子量:
567.69
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
412-920-3
Beilstein/REAXYS Number:
2406580
MDL number:
Assay:
97%
InChI key
VJDZYMIEDBLSDT-UHFFFAOYSA-N
InChI
1S/C25H29NO8S3/c1-20-4-10-23(11-5-20)35(27,28)26(16-18-33-36(29,30)24-12-6-21(2)7-13-24)17-19-34-37(31,32)25-14-8-22(3)9-15-25/h4-15H,16-19H2,1-3H3
SMILES string
Cc1ccc(cc1)S(=O)(=O)OCCN(CCOS(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c3ccc(C)cc3
assay
97%
Quality Level
mp
92-98 °C (lit.)
functional group
sulfonamide, tosylate
Application
用于制备选择性保护氮杂大环，碳桥联金属碳硼烷和四(膦酰甲基)-取代环十二烷。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
T J McMurry et al.
Bioconjugate chemistry, 4(3), 236-245 (1993-05-01)
A synthesis of the bifunctional chelator 2-(p-thiocyanatobenzyl)-1,4,7-triazacyclononane-1,4,7-triacetic acid [2-(p-NCS-Bz)-NOTA] is described which illustrates the especial utility of the (4-methoxy-2,3,6-trimethylphenyl)sulfonyl (Mtr) protecting group as an alternative to the p-tolylsulfonyl (Ts) moiety commonly used for Richman-Atkins type cyclizations. Reaction of N,N'-bis(p-tolylsulfonyl)-1-(p-benzamidobenzyl)ethylenediami ne
Rec. Trav. Chim., 110, 124-124 (1991)
The Journal of Organic Chemistry, 56, 4904-4904 (1991)
Inorganic Chemistry, 31, 3558-3558 (1992)
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