
Methyl 2-(2-bromoethyl)benzoate | CAS:25109-86-8
Methyl 2-(2-bromoethyl)benzoate
- Name:Methyl 2-(2-bromoethyl)benzoate
- CAS:25109-86-8
- Synonyms:
- Molecular Formula:C10H11BrO2
- Molecular Weight:243.10
- EINESC:
Description
Properties
Density | 1.402±0.06 g/cm3 (20 º |
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Safety
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SDS
Source | SDS/MSDS Samples |
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Synthetic Route
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More
Articles
Peer-Reviewed Papers
The use of tri-O-acetyl-D-glucal and -D-galactal in the synthesis of 3-acetamido-2,3-dideoxyhexopyranoses and -hexopyranosides.Beata Liberek et al.Carbohydrate research, 337(20), 1803-1810 (2002-11-15)
Comparison of the beta-galactosidase conformations induced by D-galactal and by magnesium ions.O M Viratelle et al.Biochemistry, 19(18), 4143-4149 (1980-09-02)
Addition of malonyl radicals to glycals with C-1 acceptor groups: remarkable influence of the substituents on the product distribution.Viktor Gyóllai et al.Chemical communications (Cambridge, England), (12)(12), 1294-1295 (2002-07-12)
Stereoselective synthesis of C-[2-S-(p-tolyl)-2-thio-beta-D-galactopyranosyl] compounds using the reaction of TolSCl adducts of D-galactal with C-nucleophiles.M Han et al.Carbohydrate research, 323(1-4), 202-207 (2000-04-27)
Totally stereoselective synthesis of 1,3-disaccharides through Diels-Alder reactions.Alessandra Bartolozzi et al.The Journal of organic chemistry, 68(22), 8529-8533 (2003-10-25)
Synthesis of new 2-phosphono-alpha-D-glycoside derivatives by stereoselective oxa-Michael addition to a D-galacto derived enone.Francesca Leonelli et al.Carbohydrate research, 343(7), 1133-1141 (2008-04-04)
Evaluation of C-(beta-D-galactosyl) and C-(2-deoxy-D-lyxo-hex-1-enopyranosyl) (D-galactal type) derivatives as inhibitors of beta-D-galactosidase from Escherichia coli.L Kiss et al.Carbohydrate research, 291, 43-52 (1996-09-23)
Stereodivergent synthesis of diastereoisomeric carba analogs of glycal-derived vinyl epoxides: a new access to carbasugars.Ileana Frau et al.Chirality, 23(9), 820-826 (2011-12-03)
A method for determination of galactosyltransferase I activity synthesizing the proteoglycan linkage region.T Higuchi et al.Journal of biochemical and biophysical methods, 29(2), 135-142 (1994-09-01)
Seeberger, P.H., et al. Aldrichimica Acta, 30, 75-75 (1997)
Direct epoxidation of D-glucal and D-galactal derivatives with in situ generated DMDO.Pavel Cheshev et al.Carbohydrate research, 341(16), 2714-2716 (2006-10-04)
[Clinical and experimental study of shuangcao tuihuang granule-1 in treating severe jaundice of acute icterohepatitis].Y X Lian et al.Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine, 21(9), 649-651 (2003-02-11)
Affinity labelling of beta-D-galactosidase from Escherichia coli with D-[6-(3)H]-galactal.G Kurz et al.Carbohydrate research, 93(1), C14-C20 (1981-06-16)
Stereochemistry of D-galactal and D-galacto-octenitol hydration by coffee bean alpha-galactosidase: insight into catalytic functioning of the enzyme.W Weiser et al.Archives of biochemistry and biophysics, 292(2), 493-498 (1992-02-01)
The use of tri-O-acetyl-D-glucal and -D-galactal in the synthesis of omega-aminoalkyl 2-deoxy- and 2,3-dideoxy-d-hexopyranosides.Anna W Pierwocha et al.Carbohydrate research, 343(15), 2680-2686 (2008-09-02)
A short and highly efficient synthesis of L-ristosamine and L-epi-daunosamine glycosides.Feiqing Ding et al.Organic letters, 13(4), 652-655 (2011-01-20)
Glycal glycosylation and 2-nitroglycal concatenation, a powerful combination for mucin core structure synthesis.Jürgen Geiger et al.The Journal of organic chemistry, 72(12), 4367-4377 (2007-05-17)
Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement.Chi-Li Chen et al.Organic letters, 11(2), 409-412 (2009-01-09)
Protic acid (HClO4 supported on silica gel)-mediated synthesis of 2,3-unsaturated-O-glucosides and a chiral furan diol from 2,3-glycals.Aditi Agarwal et al.The Journal of organic chemistry, 69(18), 6137-6140 (2004-09-18)
Remarks
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
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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