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[ CAS No. 26782-75-2 ] {[proInfo.proName]}

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Chemical Structure| 26782-75-2
Chemical Structure| 26782-75-2
Structure of 26782-75-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 26782-75-2 ]

CAS No. :26782-75-2 MDL No. :MFCD00210114
Formula : C5H9BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 181.03 Pubchem ID :-
Synonyms :

Safety of [ 26782-75-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H302-H312-H314-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 26782-75-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 26782-75-2 ]

[ 26782-75-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 72-18-4 ]
  • [ 26782-75-2 ]
YieldReaction ConditionsOperation in experiment
74% With hydrogenchloride; sodium nitrite In water
72% With hydrogen bromide; sodium nitrite In water; toluene at -5 - 20℃;
69% With hydrogen bromide; sodium nitrite In water
69% With sulfuric acid; potassium bromide; sodium nitrite at 0 - 20℃;
62% With sulfuric acid; potassium bromide; sodium nitrite at 0℃; for 1.5h; 1. Preparation of α-bromo acids 1 - 3 General procedure: To a stirred solution of an α-amino acid (1 eq.) containing potassium bromide (3 eq.) in sulfuric acid (1.5 M) at 0 °C was added sodium nitrite (1.2 eq.) portionwise over a 30 min period maintaining the temp. at or near 0 °C. The resulting solution was stirred for 1 h and then extracted with ethyl acetate (3 × 40 mL). The organic extract was dried and evaporated to give the product which was purified as stated.
59% With sulfuric acid; potassium bromide; sodium nitrite at -10℃; for 3h; Inert atmosphere; optical yield given as %ee;
55% With sulfuric acid; potassium bromide; sodium nitrite at 0℃;
With nitrosyl bromide
With hydrogen bromide
With hydrogen bromide; sodium nitrite
With hydrogen bromide; sodium nitrite at 0℃; for 4h;
With potassium bromide; sodium nitrite In sulfuric acid at 0℃; for 1h;
With sulfuric acid; potassium bromide; sodium nitrite at 0 - 5℃;
With hydrogen bromide; sodium nitrite 7 EXAMPLE 7 EXAMPLE 7 (S)-2-bromo-3-methylbutanoic acid is prepared following the procedure of Example 6 from (S)-valine and sodium nitrite and 6 N hydrogen bromide. Specific rotation of the bromo acid is [α]D25 =-17.2° (c=10% in methanol).
With sulfuric acid; potassium bromide; sodium nitrite In water at 5 - 20℃; for 5h; Cooling with ice;
With sulfuric acid; potassium bromide; sodium nitrite In water
With sulfuric acid; potassium bromide; sodium nitrite at -10℃; for 3h;
With hydrogen bromide; potassium bromide; sodium nitrite at -13℃;
With hydrogen bromide; potassium bromide; sodium nitrite at -13℃; enantiospecific reaction;
With sulfuric acid; potassium bromide; sodium nitrite at -10℃; for 6h;

Reference: [1]Lerchen, Hans-Georg; Kunz, Horst [Tetrahedron Letters, 1985, vol. 26, # 43, p. 5257 - 5260]
[2]Véniant, Murielle M.; Hale, Clarence; Hungate, Randall W.; Gahm, Kyung; Emery, Maurice G.; Jona, Janan; Joseph, Smriti; Adams, Jeffrey; Hague, Andrew; Moniz, George; Zhang, Jiandong; Bartberger, Michael D.; Li, Vivian; Syed, Rashid; Jordan, Steven; Komorowski, Renée; Chen, Michelle M.; Cupples, Rod; Kim, Ki Won; St. Jean, David J.; Johansson, Lars; Henriksson, Martin A.; Williams, Meredith; Vallgårda, Jerk; Fotsch, Christopher; Wang, Minghan [Journal of Medicinal Chemistry, 2010, vol. 53, # 11, p. 4481 - 4487]
[3]Kunz, Horst; Lerchen, Hans-Georg [Tetrahedron Letters, 1987, vol. 28, # 17, p. 1873 - 1876]
[4]Yao, Zhiyi; Du, Xiaojie; Liu, Hong; Jiang, Hualiang; Chen, Kaixian [Journal of Chemical Research, 2006, # 1, p. 3 - 5]
[5]Aitken, R. Alan; Lightfoot, Philip; Thomas, Andrew W. [Journal of Sulfur Chemistry, 2020, vol. 41, # 4, p. 369 - 387]
[6]Tanasova, Marina; Yang, Qifei; Olmsted, Courtney C.; Vasileiou, Chrysoula; Li, Xiaoyong; Anyika, Mercy; Borhan, Babak [European Journal of Organic Chemistry, 2009, # 25, p. 4242 - 4253]
[7]Kurth, Mark J.; Tahir, Hasan S.; Olmstead, Marilyn M. [Journal of Organic Chemistry, 1990, vol. 55, # 8, p. 2286 - 2288]
[8]Abderhalden; Bahn [Chemische Berichte, 1930, vol. 63, p. 915,918] Fischer,E.; Scheibler [Justus Liebigs Annalen der Chemie, 1908, vol. 363, p. 158,159][Chemische Berichte, 1908, vol. 41, p. 890,2892, 2898]
[9]Galetto,W.G.; Gaffield,W. [Journal of the Chemical Society C: Organic, 1969, p. 2437 - 2438]
[10]Stephenson,L.M.; Mattern,D.L. [Journal of Organic Chemistry, 1976, vol. 41, p. 3614 - 3619]
[11]Itsuno, Shinichi; Tanaka, Kazuo; Ito, Koichi [Chemistry Letters, 1986, p. 1133 - 1136]
[12]Sierra; Serrano; Ros; Ezcurra; Zubía [Journal of the American Chemical Society, 1992, vol. 114, # 20, p. 7645 - 7651]
[13]Saito, Kiyoshi; Harada, Kaoru [Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 8, p. 2562 - 2566]
[14]Yang; Li; Ng; Yan; Qu; Wu [Journal of Organic Chemistry, 2001, vol. 66, # 22, p. 7303 - 7312]
[15]Current Patent Assignee: Novartis (w/o Sandoz); NOVARTIS AG - US4260633, 1981, A
[16]Liu, Weiguo; Liu, Kun; Wood, Harold B.; McCann, Margaret E.; Doebber, Thomas W.; Chang, Ching H.; Akiyama, Taro E.; Einstein, Monica; Berger, Joel P.; Meinke, Peter T. [Journal of Medicinal Chemistry, 2009, vol. 52, # 14, p. 4443 - 4453]
[17]Location in patent: body text Ishihara, Jun; Watanabe, Yuki; Koyama, Noriko; Nishino, Yukihiro; Takahashi, Keisuke; Hatakeyama, Susumi [Tetrahedron, 2011, vol. 67, # 20, p. 3659 - 3667]
[18]Tanasova, Marina; Borhan, Babak [European Journal of Organic Chemistry, 2012, # 17, p. 3261 - 3269]
[19]Location in patent: scheme or table Tka, Najeh; Kraem, Jamil; Hassine, Bechir Ben [Synthetic Communications, 2012, vol. 42, # 20, p. 2994 - 3003]
[20]Tka, Najeh; Kraem, Jamil; Hassine, Bechir Ben [Synthetic Communications, 2013, vol. 43, # 5, p. 735 - 743]
[21]Panda, Siva S.; El-Nachef, Claudia; Bajaj, Kiran; Katritzky, Alan R. [European Journal of Organic Chemistry, 2013, # 19, p. 4156 - 4162]
  • 2
  • [ 26782-75-2 ]
  • [ 1310051-05-8 ]
  • [ 140-27-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: Inert atmosphere 2.1: tetrahydrofuran; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; indium(III) chloride; indium; chloro-trimethyl-silane; triethylamine / 10 - 30 °C / Inert atmosphere; Sonication 2.2: Saturated solution
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