1,3-Benzenedisulfonyl chloride | CAS:585-47-7
1,3-Benzenedisulfonyl chloride
- Name：1,3-Benzenedisulfonyl chloride
- CAS：585-47-7
- Synonyms：1,3-Phenylenebis(sulfonyl chloride); 3-(Chlorosulfonyl)benzenesulfonyl chloride; NSC 61429; m-Benzenedisulfonyl dichloride; m-Bis(chlorosulfonyl)benzene; m-Phenylenedisulfonyl chloride
- Molecular Formula：C6H4Cl2O4S2
- Molecular Weight：275.13
- EINESC：209-556-0
Description
Properties
| Melting point | 63 ºC** |
|---|---|
| Density | 1.690±0.06 g/cm3 (20 º |
Safety
| 没有数据 | 没有数据 |
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SDS
| Source | SDS/MSDS Samples |
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| 没有数据 | 没有数据 |
Synthetic Route
| Name | CAS |
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More
Articles
Peer-Reviewed Papers
Recent trends in the metabolism and cell biology of vitamin K with special reference to vitamin K cycling and MK-4 biosynthesisShearer MJ and Newman P Journal of Lipid Research, 55(3), 345-362 (2014)
Lack of effect of cefixime on the metabolism of vitamin K1.D Trenk et al.Journal of clinical pharmacology, 30(8), 737-742 (1990-08-01)
Metabolism of vitamin K1 (phylloquinone) in manBarkhan P and Shearer MJ Proceedings of the Royal Society of Medicine (1977)
Changes in the urinary metabolites of phylloquinone (vitamin K1) in man following therapeutic anticoagulation with warfarin.A McBurney et al.Biochemical pharmacology, 27(3), 273-278 (1978-02-01)
Simultaneous determination of vitamin K1, vitamin K1 2,3-epoxide and menaquinone-4 in human plasma by high-performance liquid chromatography with fluorimetric detection.K Hirauchi et al.Journal of chromatography, 430(1), 21-29 (1988-08-19)
Hereditary combined deficiency of the vitamin K-dependent clotting factorsNapolitano M, et al. Orphanet Journal of Rare Diseases, 5(1), 21-21 (2010)
Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16.Andreas Fregin et al.Blood, 100(9), 3229-3232 (2002-10-18)
miR290-5p/292-5p activate the immunoglobulin kappa locus in B cell development.Patty B Garcia et al.PloS one, 7(8), e43805-e43805 (2012-08-29)
Transcription factor USF2 is developmentally regulated in fetal lung and acts together with USF1 to induce SP-A gene expression.Erwei Gao et al.American journal of physiology. Lung cellular and molecular physiology, 284(6), L1027-L1036 (2003-02-11)
Remarks
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Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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