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123750-60-7

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123750-60-7 Usage

Uses

R-Glycidyl Nosylate is used as the chiral pool reactant to prepare C3-symmetric precursor 9.

Check Digit Verification of cas no

The CAS Registry Mumber 123750-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,5 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123750-60:
(8*1)+(7*2)+(6*3)+(5*7)+(4*5)+(3*0)+(2*6)+(1*0)=107
107 % 10 = 7
So 123750-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO6S/c11-10(12)7-1-2-9(17(13,14)15)6(3-7)4-8-5-16-8/h1-3,8H,4-5H2,(H,13,14,15)/p-1/t8-/m1/s1

123750-60-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H52366)  Glycidyl (R)-(-)-4-nitrobenzenesulfonate, 97+%   

  • 123750-60-7

  • 250mg

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H52366)  Glycidyl (R)-(-)-4-nitrobenzenesulfonate, 97+%   

  • 123750-60-7

  • 1g

  • 2352.0CNY

  • Detail
  • Alfa Aesar

  • (H52366)  Glycidyl (R)-(-)-4-nitrobenzenesulfonate, 97+%   

  • 123750-60-7

  • 5g

  • 9408.0CNY

  • Detail

123750-60-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Glycidyl (R)-(-)-4-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names (R)-(-)-Glycidyl-4-nitrobenzenesulfonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:123750-60-7 SDS

123750-60-7Relevant articles and documents

Antagonists of the calcium receptor. 2. Amino alcohol-based parathyroid hormone secretagogues

Marquis, Robert W.,Lago, Amparo M.,Callahan, James F.,Rahman, Attiq,Dong, Xiaoyang,Stroup, George B.,Hoffman, Sandra,Gowen, Maxine,DelMar, Eric G.,Van Wagenen, Bradford C.,Logan, Sarah,Shimizu, Scott,Fox, John,Nemeth, Edward F.,Roethke, Theresa,Smith, Brian R.,Ward, Keith W.,Bhatnagar, Pradip

experimental part, p. 6599 - 6605 (2010/04/03)

When administered as a single agent to rats, the previously reported calcium receptor antagonist 3 elicited a sustained elevation of plasma PTH resulting in no increase in overall bone mineral density. The lack of a bone building effect for analogue 3 was

Arenesulfonate Derivatives of Homochiral Glycidol: Versatile Chiral Building Blocks for Organic Synthesis

Klunder, Janice M.,Onami, Tetsuo,Sharpless, K. Barry

, p. 1295 - 1304 (2007/10/02)

The preparation of a series of crystalline arenesulfonate derivatives of enantiomerically enriched glycidol is described.The enhancement of optical purity by recrystallization was particularly successful for two of these derivatives, glycidyl tosylate and glycidyl 3-nitrobenzenesulfonate, which were obtained in 97 percent ee and 99 percent ee, respectively.Very high regioselectivity was observed in the reactions of these compounds with a variety of nucleophiles, including aryl oxides, Et2AlCN, organometallic reagents, and BH3-NaBH4.The application of this methodology to the synthesis of homochiral β-adrenergic blocking agents and homochiral terminal epoxides is discussed.

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