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112970-68-0

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112970-68-0 Usage

Molecular Weight

295.36 g/mol The molecular weight of the compound is 295.36 g/mol, calculated based on the atomic weights of the elements present in the compound.

Structure

Indole ring with a sulfonyl group attached to a 4-methylphenyl group and an acetate ester group The structure of the compound consists of an indole ring with a sulfonyl group attached to a 4-methylphenyl group and an acetate ester group. The sulfonyl group is a sulfur atom bonded to two oxygen atoms and an aryl or alkyl group, in this case, a 4-methylphenyl group. The acetate ester group is formed by the bonding of the carbon-oxygen double bond of the acetic acid to the hydroxyl group of the indole ring.

Physical Properties

The physical properties of 1H-Indol-4-ol, 1-[(4-methylphenyl)sulfonyl]-, acetate (ester) are not provided in the material. However, as an ester, it is likely to be a liquid or solid at room temperature with a distinct odor.

Chemical Properties

Ester reactivity, Sulfonate group reactivity As an ester, 1H-Indol-4-ol, 1-[(4-methylphenyl)sulfonyl]-, acetate (ester) can undergo hydrolysis reactions in the presence of acids or bases to form the corresponding alcohol and carboxylic acid. The presence of the sulfonyl group makes the compound more reactive towards nucleophilic substitution reactions, which is useful in organic synthesis.

Applications

Intermediate or starting material in the synthesis of pharmaceuticals and agrochemicals 1H-Indol-4-ol, 1-[(4-methylphenyl)sulfonyl]-, acetate (ester) is commonly used as an intermediate or starting material in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block for the creation of various bioactive compounds and drugs, and has potential applications in agricultural products due to its versatility and reactivity in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 112970-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112970-68:
(8*1)+(7*1)+(6*2)+(5*9)+(4*7)+(3*0)+(2*6)+(1*8)=120
120 % 10 = 0
So 112970-68-0 is a valid CAS Registry Number.

112970-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetoxy-N-tosylindole

1.2 Other means of identification

Product number -
Other names -

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112970-68-0 SDS

112970-68-0Downstream Products

112970-68-0Relevant articles and documents

Palladium-Catalyzed Coupling of 2-Bromoanilines with Vinylstannanes. A Regiocontrolled Synthesis of Substituted Indoles

Krolski, Michael E.,Renaldo, Alfred F.,Rudisill, Duane E.,Stille, J. K.

, p. 1170 - 1176 (2007/10/02)

The palladium-catalyzed cross-coupling reaction of aryl halides and triflates with vinylstannane reagents has been used to produce a variety of substituted indoles.The mild reaction conditions and selectivity inherent in the coupling reaction have been utilized to produce regiochemically pure 4-, 5-, and 6-substituted indoles.

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