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6553-96-4 | 2,4,6-Triisopropylbenzene-1-sulfonyl chloride
CAS No: 6553-96-4 Catalog No: AG0032YM MDL No:MFCD00007433
Product Description
Catalog Number:
AG0032YM
Chemical Name:
2,4,6-Triisopropylbenzene-1-sulfonyl chloride
CAS Number:
6553-96-4
Molecular Formula:
C15H23ClO2S
Molecular Weight:
302.8599
MDL Number:
MFCD00007433
IUPAC Name:
2,4,6-tri(propan-2-yl)benzenesulfonyl chloride
InChI:
InChI=1S/C15H23ClO2S/c1-9(2)12-7-13(10(3)4)15(19(16,17)18)14(8-12)11(5)6/h7-11H,1-6H3
InChI Key:
JAPYIBBSTJFDAK-UHFFFAOYSA-N
SMILES:
CC(c1cc(cc(c1S(=O)(=O)Cl)C(C)C)C(C)C)C
EC Number:
229-479-6
NSC Number:
102803
Properties
Complexity:
363
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
302.111g/mol
Formal Charge:
0
Heavy Atom Count:
19
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
302.857g/mol
Monoisotopic Mass:
302.111g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
42.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.3
Literature
| Title | Journal |
|---|---|
| Total synthesis of a cyclic adenosine 5'-diphosphate ribose receptor agonist. | The Journal of organic chemistry 20120504 |
| 2'-Azido RNA, a versatile tool for chemical biology: synthesis, X-ray structure, siRNA applications, click labeling. | ACS chemical biology 20120316 |
| Homo-C-nucleoside analogs III. Studies on the base-catalyzed dehydrative cyclization of 4-(d-manno-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole. | Carbohydrate research 20101013 |
| Enatiomerically pure hydroxycarboxylic acids: current approaches and future perspectives. | Applied microbiology and biotechnology 20100601 |
| Studies on the dehydrative cyclization of epimeric 4-(L-xylo and L-lyxo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazoles. Circular dichroism and NMR assignment of the formed anomeric C-nucleoside L-threofuranosyl triazole analogs. | Chirality 20040515 |
| Synthesis of new 3'-, 5-, and N(4)-modified 2'-O-methylcytidine libraries on solid support. | Journal of combinatorial chemistry 20030101 |
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