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1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine is a complex organic compound with a molecular formula of C27H29NO2. It features a pyrrolidine ring, which is a five-membered nitrogen-containing ring, attached to a long alkyl chain. The chain includes a phenyl group, a naphthalene ring, and a methoxy group. The naphthalene ring is part of a tetrahydro structure, indicating that it has undergone hydrogenation, reducing the number of double bonds. The compound's structure is characterized by the presence of multiple aromatic rings, which contribute to its stability and potential applications in various chemical and pharmaceutical contexts. 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine's specific structure and functional groups may endow it with unique properties that could be relevant in fields such as drug development or material science.

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  • 5879-98-1 Structure
  • Basic information

    1. Product Name: 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine
    2. Synonyms: 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine
    3. CAS NO:5879-98-1
    4. Molecular Formula:
    5. Molecular Weight: 427.587
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5879-98-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine(5879-98-1)
    11. EPA Substance Registry System: 1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine(5879-98-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5879-98-1(Hazardous Substances Data)

5879-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5879-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5879-98:
(6*5)+(5*8)+(4*7)+(3*9)+(2*9)+(1*8)=151
151 % 10 = 1
So 5879-98-1 is a valid CAS Registry Number.

5879-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1-{2-[4-(6-methoxy-2-phenyl 1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy] ethyl} pyrrolidine

1.2 Other means of identification

Product number -
Other names cis-1-{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]ethyl}pyrrolidine

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:5879-98-1 SDS

5879-98-1Relevant articles and documents

Total synthesis of lasofoxifene and nafoxidine

Umareddy, Pailla,Arava, Veera Reddy

supporting information, p. 309 - 313 (2016/04/05)

An intramolecular reductive coupling process of diketone with low-valent titanium species to form a dihydronapthalene skeleton was an important step in the synthesis of nafoxidine (1) and lasofoxifene (2). Diketone 6 was prepared in a convenient, three-st

Pharmaceutical composition having uniform drug distribution and potency

-

, (2008/06/13)

Pharmaceutical compositions having uniform drug distribution and potency utilizing laxofoxifene as an active ingredient and containing a silicon dioxide to reduce loss of the active ingredient during the manufacturing process and methods for manufacturing such compositions are disclosed.

Method for manufacturing a low dose pharmaceutical composition having uniform drug distribution and potency

-

, (2008/06/13)

A method for manufacturing a pharmaceutical composition having uniform drug distribution and potency is described which utilizes silicon dioxide to reduce the loss of active ingredient during the manufacturing process. The method is particularly useful for the manufacture of low dosage tablet compositions.

Estrogen agonists/antagonists

-

, (2008/06/13)

Compounds of formula A inhibit bone resorption and bone turnover, prevent bone loss, preserve bone strength and decrease serum cholesterol without causing prostate hypertrophy in male mammals: and E and B are selected from CH and N. R4 is H, OH, F or Cl.

Estrogen agonists/antagonists

-

, (2008/06/13)

Compounds of this formula are useful for treating or preventing, obesity, breast cancer, osteoporosis, endometriosis, cardiovascular disease and prostatic disease.

5-substitued-6-cyclic-5,6,7,8-tetrahydronaphthalen2-ol compounds which are useful for treating osteoporosis

-

, (2008/06/13)

Compounds of this formula STR1 are useful for treating or preventing, obesity, breast cancer, osteoporosis, endometriosis, cardiovascular disease and prostatic disease.

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