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2-Butyne-1,4-diol, benzoate methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164211-91-0 Structure
  • Basic information

    1. Product Name: 2-Butyne-1,4-diol, benzoate methanesulfonate
    2. Synonyms:
    3. CAS NO:164211-91-0
    4. Molecular Formula: C12H12O5S
    5. Molecular Weight: 268.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164211-91-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Butyne-1,4-diol, benzoate methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butyne-1,4-diol, benzoate methanesulfonate(164211-91-0)
    11. EPA Substance Registry System: 2-Butyne-1,4-diol, benzoate methanesulfonate(164211-91-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 164211-91-0(Hazardous Substances Data)

164211-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164211-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,2,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 164211-91:
(8*1)+(7*6)+(6*4)+(5*2)+(4*1)+(3*1)+(2*9)+(1*1)=110
110 % 10 = 0
So 164211-91-0 is a valid CAS Registry Number.

164211-91-0Relevant articles and documents

Palladium-Catalyzed Asymmetric Tandem [3+2] Cycloaddition/Allylation Reaction of Methylene-Trimethylenemethane: Access to Chiral Tricyclic Dinitrogen-Fused Heterocycles

Mao, Biming,Xu, Yi,Chen, Yuehua,Dong, Jipan,Zhang, Junya,Gu, Kejia,Zheng, Bing,Guo, Hongchao

, p. 4424 - 4427 (2019/06/27)

A palladium-catalyzed asymmetric tandem [3+2] cycloaddition/allylation of methylene-trimethylenemethane is presented, providing the functionalized chiral hexahydropyrazolo[5,1-a]isoquinoline derivatives in high yields with good to excellent enantioselecti

Method for preparing hydroxamic acids

-

Page/Page column 6, (2010/02/14)

Processes for using a compound of formula III: to make compounds of formulae I and II: and processes for making the compound of formula III, where R1-5 and J are as defined herein.

Use of hydrolases for the synthesis of cyclic amino acids

Lloyd, Richard C.,Lloyd, Michael C.,Smith, Mark E. B.,Holt, Karen E.,Swift, Jonathan P.,Keene, Philip A.,Taylor, Stephen J. C.,McCague, Raymond

, p. 717 - 728 (2007/10/03)

The synthesis of several cyclic amino acids that have all the necessary structural features to make them ideal scaffolds for use in medicinal chemistry is described. A key step in each synthesis is the use of hydrolase enzymes to define a chiral centre. I

An efficient stereoselective synthesis of Z-(2S)- and Z-(2R)-2-tert-butoxycarbonylamino-6-hydroxyhex-4-enoic acid, key intermediates in the synthesis of (2S,4S,5R)-(-)- and (2R,4R,5S)-(+)-bulgecinine

Holt, Karen E.,Swift, Jonathan P.,Smith, Mark E.B.,Taylor, Stephen J.C.,McCague, Raymond

, p. 1545 - 1548 (2007/10/03)

A concise, scaleable route to both isomers of Z-2-tert-butoxycarbonylamino-6-hydroxyhex-4-enoic acid from 2-butyne-1,4-diol, utilizing L- and D-acylase enzymes is presented. These intermediates were readily converted to multigram quantities of N-Boc-(2S,4

Novel acyclic nucleotides and nucleoside 5'-triphosphates imitating 2',3'- dideoxy-2',3'-didehydronucleotides: Synthesis and biological properties

Shirokova,Tarussova,Shipitsin,Semizarov,Krayevsky

, p. 3739 - 3748 (2007/10/02)

A series of pyrophosphoryl (Z)-(phosphonomethoxy)but-2-enyl derivatives of pyrimidines and purines 9a-d and the corresponding phosphonates 10a-d were synthesized. The prepared compounds contain the phosphonate group as an α- phosphate mimic as well as an

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