128810-31-1 Usage
Chemical class
Indole derivatives
Explanation
1H-Indol-5-yl methanesulfonate belongs to the class of compounds derived from the indole structure.
Explanation
It is a sulfonate ester formed by the condensation of indole with methanesulfonic acid.
Explanation
1H-Indol-5-yl methanesulfonate is used in organic synthesis, aiding in the construction of complex organic molecules.
Explanation
This compound is often used as a reagent in a wide range of chemical reactions due to its versatility.
Explanation
1H-Indol-5-yl methanesulfonate serves as a versatile building block for creating biologically active compounds and pharmaceuticals.
Explanation
The compound is used in the preparation of indole-based molecules for both medicinal and agricultural applications, taking advantage of its unique structure and reactivity.
Explanation
1H-Indol-5-yl methanesulfonate holds significant importance in the fields of organic chemistry and drug discovery due to its wide range of applications and its ability to create complex, biologically active molecules.
Type of compound
Sulfonate ester
Application
Organic synthesis
Use as a reagent
Various chemical reactions
Role in synthesis
Building block for biologically active compounds
Preparation of indole-based molecules
Medicinal and agricultural purposes
Importance in the field
Organic chemistry and drug discovery
Check Digit Verification of cas no
The CAS Registry Mumber 128810-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128810-31:
(8*1)+(7*2)+(6*8)+(5*8)+(4*1)+(3*0)+(2*3)+(1*1)=121
121 % 10 = 1
So 128810-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO3S/c1-14(11,12)13-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3
128810-31-1Relevant articles and documents
Concise syntheses of the amaryllidaceae alkaloids ungerimine and hippadine via the suzuki aryl-aryl cross coupling reaction
Siddiqui,Snieckus
, p. 1523 - 1526 (1990)
Short syntheses of the betaine alkaloid ungerimine (1) and the lactam alkaloid hippadine (4) based on aryl boronic acid - aryl halide cross coupling methodology are described.
A mild and efficient palladium-catalyzed cyanation of aryl mesylates in water or tBuOH/water
Yeung, Pui Yee,So, Chau Ming,Lau, Chak Po,Kwong, Fuk Yee
supporting information; experimental part, p. 8918 - 8922 (2011/02/24)
Cool and compatible: Aryl mesylates and tosylates underwent palladium-catalyzed cyanation under mild, aqueous conditions at 65-80°C (see scheme). In many cases, water could be used as the reaction medium without a cosolvent, and a variety of substituents R, such as keto, aldehyde, ester, free amine, and nitrile groups, remained intact during the transformation. Cy=cyclohexyl, Ms=methanesulfonyl, Ts=p-toluenesulfonyl.
