barbituric acid | Barbituric acid

Keyword	CPC	PCC	Volume	Score	Length of keyword
barbituric acid	0.66	0.1	7375	22	15
barbituric	1.19	0.6	3644	80	10
acid	1.28	0.3	5329	94	4

Keyword	CPC	PCC	Volume	Score
barbituric acid	0.43	0.9	8767	38
barbituric acid formula	1.25	0.8	2704	64
barbituric acid structure	1.62	0.1	5518	54
barbituric acid pka	1.28	0.1	7332	53
barbituric acid derivatives	0.86	0.4	3888	60
barbituric acid cas no	1.21	1	70	45
barbituric acid synthesis	0.22	0.7	804	13
barbituric acid sds	1.65	0.8	7535	14
barbituric acid drug	1.1	0.6	2521	54
barbituric acid chemical formula	1.33	0.1	4969	63
barbituric acid solubility	0.38	0.2	9394	55
barbituric acid molecular weight	0.61	0.2	1526	30
barbituric acid was synthesized in 1864 by	0.44	0.8	3363	52
barbituric acid was synthesized in 1864 by:	0.94	0.8	5153	14
what is barbituric acid	1.62	0.6	4660	87
1 3 dimethyl barbituric acid	0.9	0.1	4710	20
dimethyl barbituric acid	0.51	0.2	3725	80
diethyl barbituric acid	1.1	0.5	6584	37
barbituric acid uses	0.06	0.4	5747	70

Search Results related to barbituric acid on Search Engine

Barbituric acid - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Barbituric_acid

WEBBarbituric acid or malonylurea or 6-hydroxyuracil is an organic compound based on a pyrimidine heterocyclic skeleton. It is an odorless powder soluble in water. Barbituric acid is the parent compound of barbiturate drugs, although barbituric acid itself is not pharmacologically active.

DA: 41 PA: 9 MOZ Rank: 36

Barbituric acid | C4H4N2O3 | CID 6211 - PubChem
nih.gov

https://pubchem.ncbi.nlm.nih.gov/compound/Barbituric-acid

WEBMay 11, 2019 · Barbituric acid is a barbiturate, the structure of which is that of perhydropyrimidine substituted at C-2, -4 and -6 by oxo groups. Barbituric acid is the parent compound of barbiturate drugs, although it is not itself pharmacologically active. It has a role as an allergen and a xenobiotic.

DA: 10 PA: 50 MOZ Rank: 36

Barbituric Acid - an overview | ScienceDirect Topics
sciencedirect.com

https://www.sciencedirect.com/topics/chemistry/barbituric-acid

WEBJun 2, 2012 · Barbituric acid, the precursor of barbiturates, was first produced in 1864 by condensation of malonic acid and urea; it had no central nervous system (CNS) effects. In 1903, diethyl barbituric acid (barbital) was created as the first barbiturate with CNS inhibitory effects.

DA: 75 PA: 84 MOZ Rank: 13

Barbituric acid | Synthesis, Derivatives, Analgesics | Britannica
britannica.com

https://www.britannica.com/science/barbituric-acid

WEBbarbituric acid, an organic compound of the pyrimidine family, a class of compounds with a characteristic six-membered ring structure composed of four carbon atoms and two nitrogen atoms, that is regarded as the parent compound of the barbiturate drugs. It is used in the production of riboflavin, a nutritional factor

DA: 17 PA: 49 MOZ Rank: 54

Barbiturate - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Barbiturate

WEBBarbiturates are a class of depressant drugs that are chemically derived from barbituric acid. They are effective when used medically as anxiolytics , hypnotics , and anticonvulsants , but have physical and psychological addiction potential as well as overdose potential among other possible adverse effects.

DA: 11 PA: 32 MOZ Rank: 75

List of Common Barbiturates + Uses & Side Effects - Drugs.com
drugs.com

https://www.drugs.com/drug-class/barbiturates.html

WEBApr 12, 2023 · Barbiturates are a class of drugs that were used extensively in the 1960s and 1970s as a treatment for anxiety, insomnia, and seizure disorders. Apart from a few specific indications, they are not commonly prescribed these days, having been largely superseded by benzodiazepines, which are much safer, although still potentially addictive.

DA: 100 PA: 10 MOZ Rank: 36

Barbiturates - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK539731/

WEBJan 29, 2024 · Barbiturates are a category of sedative-hypnotic medications used for treating seizure disorders, neonatal withdrawal, insomnia, preoperative anxiety, and the induction of coma to address increased intracranial pressure (ICP). In addition, these medications are also helpful for inducing anesthesia.

DA: 17 PA: 24 MOZ Rank: 12

Barbituric acid - NIST Chemistry WebBook
nist.gov

https://webbook.nist.gov/cgi/cbook.cgi?ID=67-52-7

WEBBarbituric acid. Formula: C 4 H 4 N 2 O 3. Molecular weight: 128.0862. IUPAC Standard InChI: InChI=1S/C4H4N2O3/c7-2-1-3 (8)6-4 (9)5-2/h1H2, (H2,5,6,7,8,9) IUPAC Standard InChIKey: HNYOPLTXPVRDBG-UHFFFAOYSA-N. CAS Registry Number: 67-52-7. Chemical structure: This structure is also available as a 2d Mol file. Species with the …

DA: 7 PA: 28 MOZ Rank: 85

Barbiturate | Definition, Mechanism, & Side Effects | Britannica
britannica.com

https://www.britannica.com/science/barbiturate

WEBMar 28, 2024 · barbiturate, any of a class of organic compounds used in medicine as sedatives (to produce a calming effect), as hypnotics (to produce sleep), or as an adjunct in anesthesia. Barbiturates are derivatives of barbituric acid (malonyl urea), which is formed from malonic acid and urea.

DA: 10 PA: 87 MOZ Rank: 69

Barbituric acid - NIST Chemistry WebBook
nist.gov

https://webbook.nist.gov/cgi/cbook.cgi?ID=C67527&Mask=262D

WEBgas phase; Acid: barbituric acid; B Mass spectrum (electron ionization) Go To: Top , Gas phase thermochemistry data , Phase change data , Reaction thermochemistry data , Gas phase ion energetics data , UV/Visible spectrum , References , Notes

DA: 38 PA: 52 MOZ Rank: 60