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5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, (5E)-relis a complex chemical compound characterized by its unique structure and functional groups. It consists of a heptenoic acid moiety and a cyclopentyl group, with multiple stereocenters and double bonds. The presence of a chlorophenoxy group and a hydroxybutenyl group further adds to its complexity. This intricate structure is likely to confer a range of chemical and biological properties to the compound.

72029-43-7

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72029-43-7 Usage

Uses

Since the provided materials do not specify the exact applications of 5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, (5E)-rel-, it is not possible to list its uses based on the given information. However, given its complex structure and functional groups, it may potentially be used in various industries such as pharmaceuticals, materials science, or chemical research for specific applications. Further investigation and research would be required to determine its exact uses and benefits in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 72029-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72029-43:
(7*7)+(6*2)+(5*0)+(4*2)+(3*9)+(2*4)+(1*3)=107
107 % 10 = 7
So 72029-43-7 is a valid CAS Registry Number.

72029-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Cloprostenol

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:72029-43-7 SDS

72029-43-7Relevant academic research and scientific papers

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.

PROSTANOIDS. XIX. THE SYNTHESIS OF 14C-LABELED CLOPROSTENOL

Miftakhov, M. S.,Vostrikov, N. S.,Kuznetsov, O. M.,Kuvatov, Yu. G.,Murinov, Yu. I.,Tolstikov, G. A.

, p. 1072 - 1075 (2007/10/02)

A 1:3400 mixture of 2-14C-labelled methyl bromoacetate with the nonradioactive ester gave labelled dimethoxy-2-oxo-3-(m-chlorophenoxy)phosphonate which was used for the synthesis of 16-14C-labelled cloprostenol by the Corey strategy.

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