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Prostaglandin F3alpha, also known as dinoprost, is a synthetic analog of the naturally occurring prostaglandin F2alpha. It is a potent vasodilator and uterotonic agent, which means it helps to relax blood vessels and stimulate contractions in the uterus. Dinoprost is primarily used in veterinary medicine for the induction of labor in cows and as a luteolytic agent to synchronize estrous cycles in livestock. In humans, it has been used off-label for the induction of labor and the treatment of postpartum hemorrhage. It works by stimulating the production of prostaglandins in the body, which in turn leads to the desired effects on the uterus and blood vessels. Due to its potent effects, dinoprost must be used with caution and under the supervision of a healthcare professional.

745-64-2

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745-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 745-64-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 745-64:
(5*7)+(4*4)+(3*5)+(2*6)+(1*4)=82
82 % 10 = 2
So 745-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h3-4,6-7,12-13,15-19,21-23H,2,5,8-11,14H2,1H3,(H,24,25)/b6-3-,7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1

745-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name prostaglandin F3α

1.2 Other means of identification

Product number -
Other names Prostaglandin F3a

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:745-64-2 SDS

745-64-2Relevant academic research and scientific papers

Regioselective allylation and propargylation using acylsilanes: Facile synthesis of PGE3 and F(3α) methyl ester

Yanagisawa,Habaue,Yamamoto

, p. 1969 - 1980 (2007/10/02)

Regioselective allylation and propargylation were achieved using acylsilanes as electrophiles and this methodology was applied to the synthesis of PGE3 and F(3α) methyl ester.

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