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7-chloro-1,1-dimethylindan-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93904-65-5

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93904-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93904-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93904-65:
(7*9)+(6*3)+(5*9)+(4*0)+(3*4)+(2*6)+(1*5)=155
155 % 10 = 5
So 93904-65-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClO/c1-11(2)6-5-7-9(13)4-3-8(12)10(7)11/h3-4,13H,5-6H2,1-2H3

93904-65-5SDS

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 7-chloro-1,1-dimethyl-2,3-dihydroinden-4-ol

1.2 Other means of identification

Product number -
Other names EINECS 299-804-4

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:93904-65-5 SDS

93904-65-5Downstream Products

93904-65-5Relevant academic research and scientific papers

Synthesis of 1,1-dimethyl-4-indanol derivatives

Wang, Yang,Wu, Jiang,Xia, Peng

, p. 2685 - 2698 (2007/10/03)

The synthesis of 1,1-dimethyl-4-indanols (3a,b) has been achieved by intramolecular Friedel-Crafts cyclization of 2-(3-methyl-2-butenyl)phenols (5a,b) or 1-methoxy-2-(3-methyl-2-butenyl)benzenes (6a,b) followed by demethylation, respectively. It was found that the solvent was critical for the formation of different products in the intramolecular Friedel-Crafts reactions of 6. The unexpected product 4-methoxy-1,1,6,6-tetramethyl-as-hydrindacene (11) was obtained from the Friedel-Crafts reactions of 6a and its structure was confirmed by X-ray diffraction analysis. The key intermediates 5a,b were prepared by ortho-alkenylation of phenols with 1-bromo-3-methyl-2-butene, and the reaction temperature exerted an obvious impact on the yield of 2-(3-methyl-2-butenyl)phenol (5a). Copyright Taylor & Francis Group, LLC.

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