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72653-14-6

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72653-14-6 Usage

Description

4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID, also known as Tranexamic Acid, is a synthetic derivative of the amino acid lysine. It is a crucial compound in the medical field, known for its ability to inhibit the breakdown of blood clots, thus reducing the risk of excessive bleeding. This property makes it a valuable asset in treating various conditions that involve abnormal bleeding. Furthermore, its potential in treating skin hyperpigmentation by inhibiting melanin production highlights its versatility in medical applications.

Uses

Used in Surgical Procedures:
4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID is used as a hemostatic agent during surgeries to prevent excessive bleeding. Its ability to stabilize blood clots ensures that patients experience less blood loss and faster recovery times.
Used in Gynecological Applications:
In gynecology, 4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID is used as a treatment for heavy menstrual bleeding. By reducing the breakdown of blood clots, it helps manage and alleviate the symptoms associated with this condition.
Used in Emergency Medicine:
4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID is used as an emergency treatment for patients experiencing uncontrolled bleeding from various causes, such as trauma or other medical emergencies.
Used in Dermatological Applications:
4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID is used as a potential treatment for skin hyperpigmentation. Its ability to inhibit melanin production makes it a promising candidate for addressing conditions like melasma and other pigmentation disorders.
Used in Pharmaceutical Formulations:
4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID is used in the development of pharmaceutical formulations for oral, topical, or injectable administration under medical supervision, ensuring the safe and effective delivery of the compound to patients in need.
Overall, 4-ACETYL-4-(ETHOXYCARBONYL)HEPTANEDIOIC ACID plays a significant role in managing bleeding disorders and shows promise for other therapeutic applications, making it an essential component in the medical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 72653-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,5 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72653-14:
(7*7)+(6*2)+(5*6)+(4*5)+(3*3)+(2*1)+(1*4)=126
126 % 10 = 6
So 72653-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O7/c1-3-19-11(18)12(8(2)13,6-4-9(14)15)7-5-10(16)17/h3-7H2,1-2H3,(H,14,15)(H,16,17)

72653-14-6SDS

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-acetyl-4-ethoxycarbonylheptanedioic acid

1.2 Other means of identification

Product number -
Other names 4-Acetyl-4-aethoxycarbonyl-pimelinsaeure

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:72653-14-6 SDS

72653-14-6Relevant articles and documents

A Molecular Torsion Balance Study: A Nearby Anionic Group Exerts Little Influence on Hydrophobic Interactions between Nonpolar Surfaces

Ling, Xiujun,Wilcox, Craig S.

, p. 14010 - 14014 (2019/11/14)

Polar groups have a solvent ordering effect on water and therefore may affect hydrophobic binding energies for nearby lipophilic surfaces. This would mean that determinations of excess surface free energy association energies require consideration of nearby polar functional groups. This paper reports results of a study to measure this possible effect. It was concluded from the models used here that an anionic polar group nearby a hydrophobic surface has little or no effect on the magnitude of hydrophobic association.

PYRIMIDO- [4, 5-B] -OXAZINES FOR USE AS DGAT INHIBITORS

-

Page/Page column 60, (2008/06/13)

Formula (I). Compounds of formula (I) or salts thereof, wherein A1, and R1 to R5 are as defined in the specification, are DGAT-1 inhibitors and are thereby useful in the treatment of, for example, obesity. Processes to make compounds of formula (I) are also described.

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