N-Tosyl-L-alanine 3-indoxyl Ester
Original price was: $1,395.00.$695.00Current price is: $695.00.
Catalog Number: B2016125 (25 mg)
N-Tosyl-L-alanine 3-indoxyl Ester is a high quality reagent used for analyzing leukocytes, especially in urine. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
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In stock
Product Description
N-Tosyl-L-alanine 3-indoxyl Ester
Catalog number: B2016125
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 25 mg
Molecular Weight or Concentration: 358.42 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: -20°C
Keywords: Tos-Ala-Y
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.
References:
1: Mendes JA, Salustiano EJ, Pires CS, Oliveira T, Barcellos JCF, Cifuentes JMC, Costa PRR, Rennó MN, Buarque CD. 11a-N-tosyl-5-carbapterocarpans: Synthesis, antineoplastic evaluation and in silico prediction of ADMETox properties Bioorg Chem. 2018 Oct;80:585-590.
2: Shen HS, Liu N, Li ZC, Huang WC. N-Ethyl-N-phenyl-N’-tosyl-formamidine Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 17;65(Pt 7):o1582.
3: Meng XZ, Wan XJ. (E)-2-Phenyl-N-tosyl-non-2-en-4-ynamide Acta Crystallogr Sect E Struct Rep Online. 2013 Jan 1;69(Pt 1):o78.
4: Yoshioka S, Takatsuki M, Takehara T, Suzuki T, Arisawa M. Development of Cycloisomerization with Rearrangement of a Tosyl Group Using N-Tosyl-o-allenylaniline J Org Chem. 2023 Aug 4;88(15):11268-11277.
5: Lo A, Gutierrez DA, Toth-Williams G, Fettinger JC, Shaw JT. 1,3-Asymmetric Induction in Diastereoselective Allylations of Chiral N-Tosyl Imines J Org Chem. 2022 Mar 4;87(5):2773-2778.
6: Huang ML. Aqua-{N-[(4-methyl-phen-yl)sulfon-yl]glycinato(2-)-κN,O}(1,10-phenan-throline)copper(II) Acta Crystallogr Sect E Struct Rep Online. 2010 Sep 15;66(Pt 10):m1255.
7: Wu M, Hu YM. 2-Tosyl-2,3,3a,4,9,9a-hexa-hydro-1H-benzo[f]isoindol-1-one Acta Crystallogr Sect E Struct Rep Online. 2013 May 18;69(Pt 6):o926.
8: N Al-Mohammed N, Alias Y, Abdullah Z, Khaledi H. 1-Tosyl-2-[(1-tosyl-1H-benzimidazol-2-yl)methyl-sulfanyl]-1H-benzimidazole Acta Crystallogr Sect E Struct Rep Online. 2011 May 1;67(Pt 5):o1043.
9: Bennett JM, Shapiro JD, Choinski KN, Mei Y, Aulita SM, Dominguez GM, Majireck MM. Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines J Vis Exp. 2018 Jan 3;(131):56848.
10: Shi P, Tu Y, Wang C, Ma D, Bolm C. Visible Light-Promoted Synthesis of β-Keto Sulfoximines from N-Tosyl-Protected Sulfoximidoyl Chlorides J Org Chem. 2022 Mar 4;87(5):3817-3824.
Products Related to N-Tosyl-L-alanine 3-indoxyl Ester can be found at Chemicals
Additional Information
| Weight | 0.15 oz |
|---|---|
| Dimensions | 2 × 0.5 × 0.5 in |
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