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28945-95-1

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28945-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28945-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,4 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28945-95:
(7*2)+(6*8)+(5*9)+(4*4)+(3*5)+(2*9)+(1*5)=161
161 % 10 = 1
So 28945-95-1 is a valid CAS Registry Number.

28945-95-1SDS

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 6-butoxy-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 6-n-Butoxy-1-tetralon

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:28945-95-1 SDS

28945-95-1Downstream Products

28945-95-1Relevant articles and documents

PREVENTIVE AND / OR THERAPEUTIC AGENTS FOR SIP-MEDIATED DISEASES

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Paragraph 0214, (2021/04/22)

本發明之課題係提供一種將S1P5受體作動活性相對於S1P1受體作動活性之平衡經改善的化合物作為有效成份的醫藥組成物,以及將該醫藥組成物用於S1P5媒介疾病(例如,神經退化性疾病、多系統萎縮症、巴金森氏病)等之預防及/或治療的醫藥。 包含通式(V)(式中,各基的定義如說明書所載)所示之化合物或其藥學上可容許之鹽、及藥學上可容許之載體的醫藥組成物,係由於改善了S1P5受體作動活性相對於S1P1受體作動活性的平衡,故作為S1P5媒介疾病之預防及/或治療劑有用。 (式中,所有記號如說明書記載) An object

SUBSTITUTED 3,4-DIHYDRONAPHTHALENES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND PREPARATION PROCESSES

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, (2008/06/13)

Substituted 3,4-dihydronaphthalenes of the formula I wherein R1 is a methyl or an amino group, R2 represents a hydrogen atom or a methyl group, and R3 is a linear or branched chain alkyl residue having 1 to 4 carbon atoms, an allyl or a crotyl group or a cyclopentyl group are disclosed which specifically inhibit 5-lipoxygenase and are useful in pharmaceutical compositions for prophylaxis and treatment of disorders attributable to the action of leucotrienes. The dihydronaphthalenes may be prepared by reacting a compound of formula II. with hydroxylamine or a salt thereof to form the corresponding oxime, reducing the oxime to a hydroxylamine of formula III and introducing a -CO-R1 group.

Chemotherapeutic nitro-heterocyclic compounds. 3. Preparation of nitrofurfurylidene-, nitrothenylidene- and nitropyrrolylmethylene-derivatives of substituted 1-indanones and 1.2.3.4-tetrahydro-1-naphthalenones

Albrecht,Schr?der

, p. 110 - 125 (2007/10/05)

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