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40666-16-8

Fluprostenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5-Heptenoic acid,7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-,(5Z)-rel-

    Cas No: 40666-16-8

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  • 5-Heptenoic acid,7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-,(5Z)-rel-

    Cas No: 40666-16-8

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  • 40666-16-8 Structure

  • Basic information

    1. Product Name: Fluprostenol
    2. Synonyms: (+/-)-16-(3-TRIFLUOROMETHYLPHENOXY)TETRANORPROSTAGLANDIN F2ALPHA;(+/-)16-(M-TRIFLUOROMETHYLPHENOXY)-TETRANOR-PROSTAGLANDIN F2ALPHA;(+/-)-9ALPHA,11ALPHA,15R-TRIHYDROXY-16-(3-(TRIFLUOROMETHYL)PHENOXY)-17,18,19, 20-TETRANORPROSTA 5Z,13E-DIEN-1-OIC ACID;FLUPROSTENOL;(±)-16-(3-trifluoromethylphenoxy)tetranorprostaglandin f2α;FLUPROSTENOL, ETHANOL SOLUTION;(5Z)-rel-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-butenyl]cyclopentyl]-5-heptenoic acid;WWSWYXNVCBLWNZ-QIZQQNKQSA-N
    3. CAS NO:40666-16-8
    4. Molecular Formula: C23H29F3O6
    5. Molecular Weight: 458.47
    6. EINECS: 255-029-3
    7. Product Categories: N/A
    8. Mol File: 40666-16-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 608 °C at 760 mmHg
    3. Flash Point: 321.5 °C
    4. Appearance: colorless oilly liquid
    5. Density: 1.335
    6. Vapor Pressure: 1.24E-15mmHg at 25°C
    7. Refractive Index: 1.575
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: Fluprostenol(CAS DataBase Reference)
    11. NIST Chemistry Reference: Fluprostenol(40666-16-8)
    12. EPA Substance Registry System: Fluprostenol(40666-16-8)

  • Safety Data

    1. Hazard Codes: F
    2. Statements: 11
    3. Safety Statements: 7-16
    4. RIDADR: UN 1170 3/PG 2
    5. WGK Germany: 1
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 40666-16-8(Hazardous Substances Data)

40666-16-8 Usage

Uses

Fluprostenol is a prostaglandin F (FP) receptor agonist.

Check Digit Verification of cas no

The CAS Registry Mumber 40666-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40666-16:
(7*4)+(6*0)+(5*6)+(4*6)+(3*6)+(2*1)+(1*6)=108
108 % 10 = 8
So 40666-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H29F3O6/c24-23(25,26)15-6-5-7-17(12-15)32-14-16(27)10-11-19-18(20(28)13-21(19)29)8-3-1-2-4-9-22(30)31/h1,3,5-7,10-12,16,18-21,27-29H,2,4,8-9,13-14H2,(H,30,31)/t16-,18-,19-,20+,21-/m1/s1

40666-16-8 Well-known Company Product Price

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  • Sigma

  • (F8549)  Fluprostenol  10 mg/mL in ethanol, 98%

  • 40666-16-8

  • F8549-1MG

  • 1,432.08CNY

  • Detail

40666-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name fluprostenol

1.2 Other means of identification

Product number -
Other names Fluprostenol

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:40666-16-8 SDS

40666-16-8Upstream product

40666-16-8Downstream Products

40666-16-8Relevant articles and documents

Synthesis of (±) travoprost and its analogs

Mudduluru, Harikrishna,Hindupur, Rama M.,Dubey, Pramod K.,Madhavaram, Shankar,Tatini, Lakshmikumar,Subbaraju, Gottumukkala V.

experimental part, p. 234 - 241 (2012/04/18)

A new synthetic approach for the antiglaucoma agent, travoprost (1) has been developed in four steps from key intermediate (2). Key transformations include Horner-Wadsworth-Emmons reaction and separation of diastereomers to obtain (±) travoprost (1) and its analogs.

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