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862135-55-5

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862135-55-5 Usage

General Description

Acetic acid 5,6-dibromo-indan-2-yl ester is a chemical compound with the molecular formula C12H13Br2O2. It is an ester form of acetic acid and is derived from the 5,6-dibromo-indan-2-yl compound. This chemical may be used in organic synthesis or as a reagent in chemical reactions. It is important to handle this compound with care and follow proper safety procedures as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 862135-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,1,3 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 862135-55:
(8*8)+(7*6)+(6*2)+(5*1)+(4*3)+(3*5)+(2*5)+(1*5)=165
165 % 10 = 5
So 862135-55-5 is a valid CAS Registry Number.

862135-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dibromoindan-2-ol acetate

1.2 Other means of identification

Product number -
Other names 5,6-Dibromo-2,3-dihydro-1H-inden-2-yl acetate

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:862135-55-5 SDS

862135-55-5Relevant articles and documents

Method for preparing 5,6-diethyl-2,3-dihydro-1H-indene-2-amino hydrochloride

-

, (2019/10/01)

The invention relates to a novel synthesis route of a method for preparing 5,6-diethyl-2,3-dihydro-1H-indene-2-amino hydrochloride. 2-indanol is adopted as a raw material, and 5,6-diethyl-2,3-dihydro-1H-indene-2-amino hydrochloride is synthesized with a high yield through seven steps of an acetylation reaction, a substitution reaction, a coupling reaction, a hydroxyl protection reaction, a substitution reaction, a reduction reaction and a salting reaction. The preparation method of the 5,6-diethyl-2,3-dihydro-1H-indene-2-amino hydrochloride, which is provided by the invention, is a preparationmethod which is high in yield, low in cost, friendly to the environment, easy to operate and applicable to industrialization.

Concise syntheses of 2-aminoindans via indan-2-ol

G?ksu, Süleyman,Se?en, Hasan

, p. 6801 - 6807 (2007/10/03)

2-Amino-5,6-dimethoxyindan hydrochloride was synthesized in seven steps and with an overall yield of 48%. Indan-2-ol was converted to 5,6-dibromo-indan-2- ol in three steps by acetylation, electrophilic bromination and deacetylation. Dimethoxylation of 5,6-dibromoindan-2-ol with NaOCH3 in the presence of CuI gave 5,6-dimethoxy-indan-2-ol, which was converted to 2-amino-5,6-dimethoxyindan hydrochloride by azidation, followed by Pd-C catalyzed hydrogenation. Similarly, 2-amino-5-bromoindan was synthesized in five steps and with an overall yield of 50%. Indan-2-ol was converted to 2-aminoindan by azidation followed by Pd-C catalyzed hydrogenation. The reaction of 2-aminoindan with 2.5 equiv Br2 afforded 2-amino-5,6- dibromoindan.

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