salicylaldehyde, oxime structure
|
Common Name | salicylaldehyde, oxime | ||
---|---|---|---|---|
CAS Number | 94-67-7 | Molecular Weight | 137.136 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 256.5±23.0 °C at 760 mmHg | |
Molecular Formula | C7H7NO2 | Melting Point | 59-61 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 146.9±11.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of salicylaldehyde, oximeSalicylaldoxime is an organic compound, that has been used as a reagent for the gravimetric determination and separation of Cooper, Nickel, Palladium, Lead, Bismuth and Zine. The copper complex of Salicylaldoxime has anticancer activity[1][2]. |
Name | Salicylaldoxime |
---|---|
Synonym | More Synonyms |
Description | Salicylaldoxime is an organic compound, that has been used as a reagent for the gravimetric determination and separation of Cooper, Nickel, Palladium, Lead, Bismuth and Zine. The copper complex of Salicylaldoxime has anticancer activity[1][2]. |
---|---|
Related Catalog | |
In Vitro | Salicylaldoxime (300 μM) completely inhibits the relaxation activity of topoisomerase II when it forms a complex with copper; also inhibits L1210 leukaemia cell proliferation[1]. |
References |
Density | 1.2±0.1 g/cm3 |
---|---|
Boiling Point | 256.5±23.0 °C at 760 mmHg |
Melting Point | 59-61 °C(lit.) |
Molecular Formula | C7H7NO2 |
Molecular Weight | 137.136 |
Flash Point | 146.9±11.9 °C |
Exact Mass | 137.047684 |
PSA | 52.82000 |
LogP | 1.88 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.552 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | VN5775000 |
Precursor 8 | |
---|---|
DownStream 10 | |
Selective and potent agonists for estrogen receptor beta derived from molecular refinements of salicylaldoximes.
Eur. J. Med. Chem. 46 , 2453-62, (2011) In a continuing effort to improve the subtype selectivity and agonist potency of estrogen receptor β (ERβ) ligands, we have designed and developed a thus far unexplored structural series obtained by m... |
|
Structural evolutions of salicylaldoximes as selective agonists for estrogen receptor beta.
J. Med. Chem. 52 , 858-67, (2009) The bioisosteric replacement of the phenol ring, a signature functional group of most estrogen receptor (ER) ligands, with a hydrogen-bonded pseudocyclic ring, led to the development of a novel class ... |
|
Linking [M(III)3] triangles with "double-headed" phenolic oximes.
Dalton Trans. 41(29) , 8777-85, (2012) Strapping two salicylaldoxime units together with aliphatic α,Ω-aminomethyl links in the 3-position gives ligands which allow the assembly of the polynuclear complexes [Fe(7)O(2)(OH)(6)(H(2)L1)(3)(py)... |
2-hydroxybenzaldehyde oxime |
salicylaldehyde, oxime |
Saldox |
Benzaldehyde, 2-hydroxy-, oxime |
SALICYLALDEHYDE OXIME |
Salicylaldehydoxime |
2-hydroxybenzaldoxime |
SalicyladoximeGr |
o-Hydroxybenzaldoxime |
MFCD00002120 |
o-hydroxybenzaldehyde oxime |
EINECS 202-353-8 |
2-[(Hydroxyimino)methyl]phenol |
Salicaldehyde oxime |
2-[(E)-(Hydroxyimino)methyl]phenol |