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1H-Indole-4-carboxaldehyde, 1-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79681-04-2 Structure
  • Basic information

    1. Product Name: 1H-Indole-4-carboxaldehyde, 1-[(4-methylphenyl)sulfonyl]-
    2. Synonyms:
    3. CAS NO:79681-04-2
    4. Molecular Formula: C16H13NO3S
    5. Molecular Weight: 299.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79681-04-2.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: 1H-Indole-4-carboxaldehyde, 1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole-4-carboxaldehyde, 1-[(4-methylphenyl)sulfonyl]-(79681-04-2)
    11. EPA Substance Registry System: 1H-Indole-4-carboxaldehyde, 1-[(4-methylphenyl)sulfonyl]-(79681-04-2)
  • 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: 79681-04-2(Hazardous Substances Data)

79681-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79681-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,8 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79681-04:
(7*7)+(6*9)+(5*6)+(4*8)+(3*1)+(2*0)+(1*4)=172
172 % 10 = 2
So 79681-04-2 is a valid CAS Registry Number.

79681-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)sulfonylindole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-tosylindole-4-carboxaldehyde

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:79681-04-2 SDS

79681-04-2Relevant articles and documents

Enantioselective alkenylation of aldimines catalyzed by a rhodium-diene complex

Cui, Zhe,Chen, Ya-Jing,Gao, Wen-Yun,Feng, Chen-Guo,Lin, Guo-Qiang

, p. 1016 - 1019 (2014)

An efficient rhodium-catalyzed asymmetric addition reaction of potassium alkenyltrifluoroborates to N-nosylaldimines has been developed. Under optimal conditions, the reactions proceeded with good to excellent yields and excellent enantioselectivities (97

Syntheses of Polycyclic Tetrahydrofurans by Cascade Reactions Consisting of Five-Membered Ring Selective Prins Cyclization and Friedel-Crafts Cyclization

Sakata, Yuki,Yasui, Eiko,Takatori, Kazuhiko,Suzuki, Yuji,Mizukami, Megumi,Nagumo, Shinji

, p. 9103 - 9118 (2018/07/21)

A novel cascade reaction consisting of a five-membered ring selective Prins cyclization and a subsequent Friedel-Crafts cyclization is reported. Treatment of homocinnamyl alcohols and aromatic aldehydes with BF3·OEt2 in CH2/sub

Switching the regioselectivity via indium(iii) and gold(i) catalysis: A post-Ugi intramolecular hydroarylation to azepino- and azocino-[c,d]indolones

Kumar, Amit,Li, Zhenghua,Sharma, Sunil K.,Parmar, Virinder S.,Van Der Eycken, Erik V.

supporting information, p. 6803 - 6805 (2013/07/26)

A post-Ugi indium(iii)- and gold(i)-mediated regioselective intramolecular hydroarylation for the synthesis of azepino- and azocino-[c,d]indolones is described.

SERINE/THREONINE PAK1 INHIBITORS

-

Page/Page column 127-128, (2013/03/26)

Compounds having the formula I wherein A, Z, R1a, R1b, R2, R3, R4, R5, R6, R7, R9, R10, Ra, Rb and n are as defined herein are inhibitors of PAK1. Also disclosed are compositions and methods for treating cancer and hyperproliferative disorders.

INDOLES AS 5-HT6 MODULATORS

-

Page/Page column 65-66, (2008/06/13)

The present invention relates to novel compounds of formula (I) wherein m, n, R0, R1, R2, R3 and R4 are as described herein, to pharmaceutical compositions comprising the compounds, to processes for t

Thiazolidinedione derivatives, method for preparing the derivatives and pharmaceutical compositions containing same

-

, (2008/06/13)

A thiazolidinedione derivative represented by the following general formula (I): STR1 ?wherein the dotted line represents a single bond or a double bond, the thiazolidinedione ring residue is linked to either of 2-, 3-, 4-, 5- and 6-positions on the indole ring and R represents a group selected from the group consisting of hydrogen atom and alkyl, alkenyl, alkynyl, phenyl, aralkyl, heterocycloalkyl, arylsulfonyl and arylaminocarbonyl groups! or a pharmaceutically acceptable salt thereof exhibits excellent effects of reducing the blood sugar level and of reducing the lipid concentration in blood and is accordingly useful as a therapeutic agent for treating diabates mellitus. These derivatives and pharmaceutically acceptable salt thereof are almost free of any side effect.

4-benzyl-1H-indoles and anti-arrthymic use thereof

-

, (2008/06/13)

Novel 4-benzyl-1H-indoles of the formula STR1 in all diastereoisomeric forms and mixtures thereof having antiarhythmic activity.

3-oxadiazole and 3-carboxylic acid beta-carboline derivatives, and their use as psychotropic agents

-

, (2008/06/13)

Compounds of formula I STR1 wherein X is COOR 3 or an oxadiazolyl radical of the formula orR 2 is H, lower alkyl or cycloalkyl,R 3 is lower alkyl,R 4 is hydrogen, lower alkyl or lower alkoxyalkyl,R A is -CHR 1 -Z-R 5,Z is sulfur or oxygen,R 1 is lower alk

SHORT STEP SYNTHESIS OF 4-FORMYLINDOLE AND DERIVATIVES FROM 4-OXO-4,5,6,7-TETRAHYDROINDOLE

Hatanaka, Naoto,Watanabe, Nobuko,Matsumoto, Masakatsu

, p. 1987 - 1996 (2007/10/02)

The reaction of 4-oxo-4,5,6,7-tetrahydroindole with umpolung anions provides a new short efficient procedure for the synthesis of 4-formylindole derivatives.

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