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1729-38-0

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1729-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1729-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1729-38:
(6*1)+(5*7)+(4*2)+(3*9)+(2*3)+(1*8)=90
90 % 10 = 0
So 1729-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H20O2/c1-25-20-12-14-22-18(15-20)9-13-21(16-5-3-2-4-6-16)23(22)17-7-10-19(24)11-8-17/h2-8,10-12,14-15,24H,9,13H2,1H3

1729-38-0SDS

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 4-(6-methoxy-2-phenyl-3,4-dihydronaphthalen-1-yl)phenol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1729-38-0 SDS

1729-38-0Relevant articles and documents

An expeditious synthesis of lasofoxifene and nafoxidine via the novel three-component coupling reaction

Sano, Yoshiyuki,Nakata, Kenya,Otoyama, Takafumi,Umeda, Sei,Shiina, Isamu

, p. 40 - 41 (2007)

The simple and efficient synthesis of lasofoxifene (4), a possible candidate for alleviating osteoporosis, via the novel three-component coupling reaction among 4-pivaloyloxybenzaldehyde (5), cinnamyltrimethylsilane (6), and anisole in the presence of HfCl4 is illustrated. The successive cationic cyclization of the coupling product, olefin formation, and migration of the double-bond are performed to afford the common synthetic intermediate of lasofoxifene (4) and nafoxidine (3) via a very concise procedure. Copyright

NOVEL DIHYDRONAPHTHALENE COMPOUND AND USE THEREOF

-

Page/Page column 18-19, (2010/06/17)

Disclosed is a compound represented by the formula (I) below as a dihydronaphthalene compound having a chemical structure which is excellent in production efficiency when compared with lasofoxifene and nafoxidine. This compound is useful as a proteasome i

PROCESS FOR PRODUCTION OF LASOFOXIFENE OR ANALOGUE THEREOF

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Page/Page column 19-20; 30, (2008/12/04)

Disclosed is a novel process for production of lasofoxifene, nafoxidine or an analogue thereof, which comprises reduced number of reaction steps, has a high efficiency, and is practically advantageous. For the production of lasofoxifene or an analogue the

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