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899-79-6

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899-79-6 Usage

General Description

2-[(2E)-2-(6-methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)ethyl]-2-methylcyclopentane-1,3-dione is a chemical compound with a complex molecular structure. It contains a cyclopentane-1,3-dione core with a side chain consisting of a 6-methoxy-3,4-dihydronaphthalen-1(2H)-ylidene group and a methyl group. 2-[(2E)-2-(6-methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)ethyl]-2-methylcyclopentane-1,3-dione is likely to have pharmacological properties due to its structural resemblance to other known bioactive compounds. However, further research and analysis are needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 899-79-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 899-79:
(5*8)+(4*9)+(3*9)+(2*7)+(1*9)=126
126 % 10 = 6
So 899-79-6 is a valid CAS Registry Number.

899-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(6-methoxy-3,4-dihydro-2H-naphthalen-1-ylidene)ethyl]-2-methylcyclopentane-1,3-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:899-79-6 SDS

899-79-6Relevant articles and documents

Zn-Mediated Hydrodeoxygenation of Tertiary Alkyl Oxalates

Ye, Yang,Ma, Guobin,Yao, Ken,Gong, Hegui

, p. 1625 - 1628 (2021/01/18)

Herein we describe a general, mild, and scalable method for hydrodeoxygenation of readily accessible tertiary alkyl oxalates by Zn/silane under Ni-catalyzed conditions. The reduction method is suitable for an array of structural motifs derived from tertiary alcohols that bear diverse functional groups, including the synthesis of a key intermediate en route to estrone.

Desymmetrization of cyclic 1,3-diketones via Ir-catalyzed hydrogenation: An efficient approach to cyclic hydroxy ketones with a chiral quaternary carbon

Gong, Quan,Wen, Jialin,Zhang, Xumu

, p. 6350 - 6353 (2019/07/04)

We herein report an efficient method to synthesize cyclic hydroxy ketones with a chiral quaternary center. Catalyzed by an Ir/f-ampha complex, cyclic α,α-disubstituted 1,3-diketones were hydrogenated, giving mono-reduced products with both high enantiosel

Pentacyclic compounds by samarium diiodide-induced cascade cyclizations of naphthyl-substituted 1,3-diones

Wefelscheid, Ulrike K.,Reissig, Hans-Ulrich

supporting information; scheme or table, p. 65 - 69 (2009/04/06)

Treatment of naphthyl-substituted cyclopentane-1,3-diones with the samarium diiodidehexamethylphosphoramide (HMPA) complex in the presence of tert-butyl alcohol provided the expected tetracyclic diols with steroid-like structures. Surprisingly, reactions

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