Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate
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Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate
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CAS No:
14394-26-4
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Formula:
C8H17O4P
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Chemical Name:
Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate
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Synonyms:
Phosphonic acid,P-(1,1-dimethyl-3-oxobutyl)-,dimethyl ester;Phosphonic acid,(1,1-dimethyl-3-oxobutyl)-,dimethyl ester;Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate;Dimethyl (1,1-dimethyl-3-oxobutyl)phosphonate;Dimephosphon;Mitsefosfon;Dimephosphone;86003-41-0
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CAS No:
Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate Basic Attributes
208.192
208.19
136CQC28US
DTXSID20162578
Drug Information
Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)|Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)|Various agents with different action mechanisms used to treat or ameliorate PEPTIC ULCER or irritation of the gastrointestinal tract. This has included ANTIBIOTICS to treat HELICOBACTER INFECTIONS; HISTAMINE H2 ANTAGONISTS to reduce GASTRIC ACID secretion; and ANTACIDS for symptomatic relief. (See all compounds classified as Anti-Ulcer Agents.)|Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)|Substances that counteract or neutralize acidity of the GASTROINTESTINAL TRACT. (See all compounds classified as Antacids.)|Agents counteracting or neutralizing the action of POISONS. (See all compounds classified as Antidotes.)
(1,1-dimethyl-3-oxobutyl)phosphonic acid dimethyl ester
Computed Properties
Molecular Weight:208.19
XLogP3:-0.3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:208.08644602
Monoisotopic Mass:208.08644602
Topological Polar Surface Area:52.6
Heavy Atom Count:13
Complexity:226
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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Dimethyl P-(1,1-dimethyl-3-oxobutyl)phosphonate
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