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Methyldopate, also known as Methyldopa Hydrochloride, is a synthetic derivative of the naturally occurring amino acid dopa. It is a white crystalline powder with a slightly bitter taste. Methyldopate is primarily used in the medical field for its hypotensive properties, which help lower blood pressure. It works by stimulating the production of certain neurotransmitters in the brain, leading to a reduction in peripheral vascular resistance and, consequently, a decrease in blood pressure.

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  • 6014-30-8 Structure
  • Basic information

    1. Product Name: methyldopate
    2. Synonyms: methyldopa ethyl;methyldopate;ethyl 2-amino-3-(3,4-dihydroxyphenyl)-2-methyl-propanoate;Alanine, 3-(3,4-dihydroxyphenyl)-2-methyl-, ethyl ester, L-;L-3-(3,4-Dihydroxyphenyl)-2-methylalanine ethyl ester;SVEBYYWCXTVYCR-LBPRGKRZSA-N
    3. CAS NO:6014-30-8
    4. Molecular Formula: C12H17NO4
    5. Molecular Weight: 239.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6014-30-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 398°C at 760 mmHg
    3. Flash Point: 194.5°C
    4. Appearance: /
    5. Density: 1.243g/cm3
    6. Vapor Pressure: 6.62E-07mmHg at 25°C
    7. Refractive Index: 1.572
    8. Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
    9. Solubility: DMSO (Slightly, Heated), Methanol (Slightly)
    10. PKA: 9.83±0.10(Predicted)
    11. Stability: Hygroscopic
    12. CAS DataBase Reference: methyldopate(CAS DataBase Reference)
    13. NIST Chemistry Reference: methyldopate(6014-30-8)
    14. EPA Substance Registry System: methyldopate(6014-30-8)
  • 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: 6014-30-8(Hazardous Substances Data)

6014-30-8 Usage

Uses

Used in Pharmaceutical Industry:
Methyldopate is used as an antihypertensive agent for the treatment of hypertension. It is particularly effective in managing high blood pressure during pregnancy, as it has been shown to have minimal effects on the fetus. The hypotensive effects of methyldopate make it a valuable drug for managing various cardiovascular conditions.
Used in Oncology:
Methyldopate has been found to be effective in the treatment of murine neural blastoma, a type of cancer that affects the nervous system. Its application in oncology is still being researched, but the initial findings suggest that it may have potential as a therapeutic agent for certain types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 6014-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6014-30:
(6*6)+(5*0)+(4*1)+(3*4)+(2*3)+(1*0)=58
58 % 10 = 8
So 6014-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO4/c1-3-17-11(16)12(2,13)7-8-4-5-9(14)10(15)6-8/h4-6,14-15H,3,7,13H2,1-2H3

6014-30-8Downstream Products

6014-30-8Relevant articles and documents

Salvianolic acid A analogue and application thereof as antioxidant

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Paragraph 0042-0043; 0045, (2020/01/12)

The invention provides a novel salvianolic acid A analogue with antioxidant activity. The ROS can be directly or indirectly eliminated by up-regulating expression of CAT, SOD and like antioxidase andincreasing the production of the non-enzymatic antioxida

Memory of chirality of tertiary aromatic amide: Application to the asymmetric synthesis of (S)-α-methylDOPA

Mai, Thi Thoa,Viswambharan, Baby,Gori, Didier,Kouklovsky, Cyrille,Alezra, Valerie

, p. 8797 - 8801,5 (2020/09/15)

We describe an original asymmetric synthesis of (S)-α-methylDOPA proceeding by the concept of memory of chirality, the only source of chirality being the starting d-alanine. The initial chirality of the amino acid is temporarily transferred to a dynamic axial chirality of a tertiary aromatic amide. The (S)-α-methylDOPA hydrochloride is obtained after four steps with 98% ee.

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