Ancymidol structure
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Common Name | Ancymidol | ||
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CAS Number | 12771-68-5 | Molecular Weight | 256.30000 | |
Density | 1.259 g/cm3 | Boiling Point | 442.2ºC at 760 mmHg | |
Molecular Formula | C15H16N2O2 | Melting Point | 110-111°C | |
MSDS | Chinese USA | Flash Point | 221.2ºC |
Use of AncymidolAncymidol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | ancymidol |
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Synonym | More Synonyms |
Description | Ancymidol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.259 g/cm3 |
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Boiling Point | 442.2ºC at 760 mmHg |
Melting Point | 110-111°C |
Molecular Formula | C15H16N2O2 |
Molecular Weight | 256.30000 |
Flash Point | 221.2ºC |
Exact Mass | 256.12100 |
PSA | 55.24000 |
LogP | 2.13110 |
Vapour Pressure | 1.35E-08mmHg at 25°C |
Index of Refraction | 1.618 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | UV9280000 |
HS Code | 2933599016 |
~31% Ancymidol CAS#:12771-68-5 |
Literature: REGENTS OF THE UNIVERSITY OF MINNESOTA; VINCE, Robert; VARTAK, Ashish P. Patent: WO2012/128965 A2, 2012 ; Location in patent: Page/Page column 15 ; |
~43% Ancymidol CAS#:12771-68-5 |
Literature: Taylor, Harold M.; Jones, C. David; Davenport, James D.; Hirsch, Kenneth S.; Kress, T.J.; Weaver, Dix Journal of Medicinal Chemistry, 1987 , vol. 30, # 8 p. 1359 - 1365 |
~% Ancymidol CAS#:12771-68-5 |
Literature: WO2012/128965 A2, ; |
~% Ancymidol CAS#:12771-68-5 |
Literature: WO2012/128965 A2, ; |
HS Code | 2933599016 |
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Summary | 2933599016 cyclopropyl(4-methoxyphenyl)(pyrimidin-5-yl)methanol。supervision conditions:s(import or export registration certificate for pesticides)。VAT:17.0%。tax rebate rate:9.0%。MFN tarrif:6.5%。general tariff:20.0% |
Apoptolidins A and C activate AMPK in metabolically sensitive cell types and are mechanistically distinct from oligomycin A.
Biochem. Pharmacol. 93(3) , 251-65, (2015) Apoptolidin A was first isolated as a secondary metabolite of a Nocardiopsis sp. and is the founding member of a family of potential selective cancer cell toxins. We now report the isolation, producti... |
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Involvement of gibberellin in tracheary element differentiation and lignification in Zinnia elegans xylogenic culture.
Protoplasma 228(4) , 179-87, (2006) Gibberellin (GA) is considered an important growth regulator involved in many aspects of plant development. However, little is known about the relationship between GA and lignification. In this study,... |
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A novel, cellulose synthesis inhibitory action of ancymidol impairs plant cell expansion.
J. Exp. Bot. 59 , 3963-3974, (2008) The co-ordination of cell wall synthesis with plant cell expansion is an important topic of contemporary plant biology research. In studies of cell wall synthesis pathways, cellulose synthesis inhibit... |
A-Rest Solution |
reducymol |
Ancymidol |
EINECS 235-814-7 |
α-cyclopropyl-α-(4-methoxyphenyl)-5-pyrimidinemethanol |
rac-(R)-cyclopropyl(4-methoxyphenyl)(pyrimidin-5-yl)methanol |
A-REST |
Thritone |
el-531 |
MFCD00072501 |
(RS)-α-cyclopropyl-4-methoxy-α-(pyrimidin-5-yl)benzyl alcohol |
quel |