737000-84-9

Basic information

• Product Name: (S)-(+)-1-INDANYL ISOTHIOCYANATE
• Synonyms: (S)-(+)-1-INDANYL ISOTHIOCYANATE;(S)-1-isothiocyanato-2,3-dihydro-1H-indene
• CAS NO: 737000-84-9
• Molecular Formula: C10H9NS
• Molecular Weight: 175.25
• Mol File: 737000-84-9.mol

Chemical Properties

• Boiling Point: 108-113°C 0,1mm
• Flash Point: 108-113°C/0.1mm
• Appearance: /
• Density: 1,146 g/cm3
• Refractive Index: 1.6130
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: (S)-(+)-1-INDANYL ISOTHIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-1-INDANYL ISOTHIOCYANATE(737000-84-9)
• EPA Substance Registry System: (S)-(+)-1-INDANYL ISOTHIOCYANATE(737000-84-9)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 2810
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 737000-84-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Medicinal Applications:
(S)-(+)-1-Indanyl isothiocyanate is used as a pharmaceutical agent for its potential anticancer properties. Preclinical studies have shown that it exhibits promising effects against various types of cancer, making it a candidate for further research and development in the field of oncology.
(S)-(+)-1-Indanyl isothiocyanate is also used as an anti-inflammatory agent due to its demonstrated ability to reduce inflammation in preclinical studies. This property makes it a potential candidate for the development of new treatments for inflammatory diseases.
Used in Flavoring and Fragrance Industry:
(S)-(+)-1-Indanyl isothiocyanate is used as a flavoring agent in the food and beverage industry. Its unique chemical structure contributes to the development of novel flavors, enhancing the taste profiles of various products.
(S)-(+)-1-Indanyl isothiocyanate is used as a fragrance agent in the cosmetics and perfumery industry. Its distinct chemical properties allow for the creation of new and innovative scents, adding value to fragrance formulations.

Upstream product

• 463-56-9 thiocyanic acid 
• 95-13-6 1-indene 
• 2290-65-5 trimethylsilyl isothiocyanate 
• 496-11-7 INDANE 
• 463-71-8 thiophosgene 
• 34698-41-4 2,3-dihydro-1H-inden-1-amine 
• 60212-02-4 trans-2-iodo-1-isothiocyanato-indan 

Relevant articles and documents

Electrochemical Benzylic C(sp3)-H Isothiocyanation

Selective C(sp3)-H isothiocyanation represents a significant strategy for the synthesis of isothiocyanate derivatives. We report herein an electrochemical benzylic isothiocyanation in a highly chemo- and site-selective manner under external oxidant-free conditions. The high chemoselectivity is attributed to the facile in situ isomerization of benzylic thiocyanates to isothiocyanates. Notably, the method exhibits high functional group compatibility and is suitable for late-stage functionalization of bioactive molecules.

CHEMICAL COMPOUNDS

A compound of formula (I) where the substituents have the meanings assigned to them in claim 1 , compositions comprising a compound of formula (I) and the use of such compounds and/or compositions controlling insects, acarines, nematodes or molluscs.

INDANYL-AND TETRAHYDRONAPHTYL-AMINO-THIOUREA COMPOUNDS FOR COMBATING ANIMAL PESTS

Indanyl- and Tetrahydronaphtyl-amino-thiourea compounds for combating animal pests The present invention relates to Indanyl- and Tetrahydronaphtyl-amino-thiourea compounds of formula I wherein the variables R1 to R4 are as in the des

ALKYL AND ARYL ISOTHIOCYANATES AS MASKED PRIMARY AMINES

Primary and secondary (but not tertiary) alkyl as well as aryl isothiocyanates react rapidly with 4-methyl-1,2-benzenedithiol (1) in methanol at room temperature, releasing the corresponding amines in good yields.This mild and simple procedure for unmasking amines proceeds chemospecifically with isothiocyanates even in the presence of such normally electrophilic and reactive functionalities as carboxylate ester and N-alkylphthalimide.