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(1,3,3-TRIMETHYL-2-METHYLENE-2,3-DIHYDRO-1H-INDOL-6-YL)-METHANOL is a complex chemical compound that is a derivative of indole, a naturally occurring compound found in many plants and animals. As a methanol derivative, it contains a methanol group in its structure. (1,3,3-TRIMETHYL-2-METHYLENE-2,3-DIHYDRO-1H-INDOL-6-YL)-METHANOL is of interest to scientists and researchers due to its potential medicinal properties and unique structure.
Used in Research and Pharmaceutical Applications:
(1,3,3-TRIMETHYL-2-METHYLENE-2,3-DIHYDRO-1H-INDOL-6-YL)-METHANOL is used as a research and pharmaceutical compound for its potential medicinal properties. Its unique structure and properties make it a valuable subject for scientific study and exploration in various fields.

143445-60-7

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143445-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143445-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,4 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143445-60:
(8*1)+(7*4)+(6*3)+(5*4)+(4*4)+(3*5)+(2*6)+(1*0)=117
117 % 10 = 7
So 143445-60-7 is a valid CAS Registry Number.

143445-60-7SDS

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 (1,3,3-trimethyl-2-methylideneindol-6-yl)methanol

1.2 Other means of identification

Product number -
Other names 1H-Indole-6-methanol,2,3-dihydro-1,3,3-trimethyl-2-methylene

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:143445-60-7 SDS

143445-60-7Downstream Products

143445-60-7Relevant academic research and scientific papers

Preparation of a conjugation-ready thiol responsive molecular switch

Tautges, Brandon,Or, Victor,Garcia, Joel,Shaw, Jared T.,Louie, Angelique Y.

supporting information, p. 6569 - 6573 (2015/11/09)

In this work we synthesize molecular switches that are responsive to cysteine, homocysteine, and glutathione; three redox systems that make up the majority of the body's antioxidant defenses. Synthesized spiropyran isomers with conjugation-ready linkages

PHOTOCHROMIC PROBES

-

Page/Page column 46; 47; 49, (2008/06/13)

The present invention provides photochromic compounds and derivatives thereof as shown in claim 1 and methods of use of these compounds and derivatives. The present invention also provides photochromic optical probes capable of undergoing light directed r

Family of site-selective molecular optical switches

Sakata, Tomoyo,Yan, Yuling,Marriott, Gerard

, p. 2009 - 2013 (2007/10/03)

(Chemical Equation Presented) We describe the design, synthesis, and characterization of a family of thiol-reactive optical switches for labeling proteins and other biomolecules. Site-selective introduction of photochromic probes within biomolecules is be

Alkali-Metal Cation Recognition Induced Isomerization of Spirobenzopyrans and Spironaphthoxazins Possessing a Crown Ring as a Recognition Site: Multifunctional Artificial Receptors

Inouye, Masahiko,Ueno, Masaru,Tsuchiya, Kikuo,Nakayama, Naomi,Konishi, Takashi,Kitao, Teijiro

, p. 5377 - 5383 (2007/10/02)

Spirobenzopyrans and spironaphthoxazins possessing a monoaza-crown ring were synthesized.Isomerization of these compounds to the open colored merocyanines was induced by recognition of alkali-metal cations and the selectivity of the coloration was found to be governed by several factors: (1) the size of the crown ring, (2) the position of recognition, (3) electric properties of both the complexed cations and the merocyanine dipoles, and (4) the length of the alkyl chains connecting the spirobenzopyran units and the crown units.The spirobenzopyrans represent rationally designed multifunctional receptors for alkali-metal cations.

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