Structure of 3724-26-3
*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
4.5
*For Research Use Only !
Change View
Size | Price | VIP Price | US Stock |
Global Stock |
In Stock | ||
{[ item.pr_size ]} |
Inquiry
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.discount_usd) ]} {[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} |
Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]} | Inquiry {[ item.pr_usastock ]} In Stock Inquiry - | {[ item.pr_chinastock ]} {[ item.pr_remark ]} In Stock 1-2 weeks - Inquiry - | Login | - + | Inquiry |
Please Login or Create an Account to: See VIP prices and availability
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
1-2weeks
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price, item.pr_usd) ]}
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
In Stock
- +
Please Login or Create an Account to: See VIP prices and availability
US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Henesey, Brian P ; Ingwer, Stephanie M ; Tracey, Hope S ; Obarow, Elizabeth G ; Holappa, Rachael E ; King, Adelaide M , et al.
Abstract: The formation of brown carbon (BrC) in aqueous atmospheric aerosols is well-documented and often attributed to aldehyde-ammonia reactions. However, many studies have focused on individual aldehyde precursors, overlooking the complex composition of organic aerosols, which comprise a diverse mix of organic and inorganic compounds. To address this, a complex BrC system was investigated by generating aqueous atmospheric aerosol mimics containing glyoxal (Gly), glycolaldehyde (GAld), and ammonium sulfate. Structural analysis using supercritical fluid chromatography−mass spectrometry (SFC-MS) showed that adjusting the Gly:GAld mole ratio leads to variations in the composition and abundance of BrC products formed. Notably, aromatic heterocycles (e.g., imidazoles and pyrazines) as well as acyclic carbonyl oligomers were identified to form at different concentrations depending on the Gly:GAld mole ratio. UV−visible spectroscopy analysis demonstrated that light absorption in these mixed Gly + GAld + AS systems cannot be modeled as a simple weighted average of the Gly:GAld mole ratio; observed changes in light absorbance can be explained by compositional changes in solution. These observations indicate that cross-reactions are occurring between the Gly and GAld in solution, potentially leading to changes in the physical properties of the aerosol. Given the thousands of reactive compounds found in atmospheric aerosol, these findings could have important implications for our understanding of organic reactions within the aerosol.
Show More >
Keywords: Brown carbon ; carbonyl cross-reactions ; glyoxal ; glycolaldehyde ; pyrazines ; imidazoles
Show More >
CAS No. : | 3724-26-3 |
Formula : | C4H6N2O |
M.W : | 98.10 |
SMILES Code : | OCC1=NC=CN1 |
MDL No. : | MFCD06202766 |
InChI Key : | ZOMATQMEHRJKLO-UHFFFAOYSA-N |
Pubchem ID : | 566830 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H332-H335 |
Precautionary Statements: | P280-P305+P351+P338-P310 |
Num. heavy atoms | 7 |
Num. arom. heavy atoms | 5 |
Fraction Csp3 | 0.25 |
Num. rotatable bonds | 1 |
Num. H-bond acceptors | 2.0 |
Num. H-bond donors | 2.0 |
Molar Refractivity | 24.72 |
TPSA ? Topological Polar Surface Area: Calculated from |
48.91 Ų |
Log Po/w (iLOGP)? iLOGP: in-house physics-based method implemented from |
0.74 |
Log Po/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by |
-0.79 |
Log Po/w (WLOGP)? WLOGP: Atomistic method implemented from |
-0.25 |
Log Po/w (MLOGP)? MLOGP: Topological method implemented from |
-1.35 |
Log Po/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by |
0.9 |
Consensus Log Po/w? Consensus Log Po/w: Average of all five predictions |
-0.15 |
Log S (ESOL):? ESOL: Topological method implemented from |
-0.41 |
Solubility | 37.9 mg/ml ; 0.386 mol/l |
Class? Solubility class: Log S scale |
Very soluble |
Log S (Ali)? Ali: Topological method implemented from |
0.24 |
Solubility | 171.0 mg/ml ; 1.74 mol/l |
Class? Solubility class: Log S scale |
Highly soluble |
Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by |
-0.98 |
Solubility | 10.2 mg/ml ; 0.104 mol/l |
Class? Solubility class: Log S scale |
Soluble |
GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg |
High |
BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg |
No |
P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) |
No |
CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) |
No |
CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) |
No |
CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) |
No |
CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) |
No |
CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) |
No |
Log Kp (skin permeation)? Skin permeation: QSPR model implemented from |
-7.46 cm/s |
Lipinski? Lipinski (Pfizer) filter: implemented from |
0.0 |
Ghose? Ghose filter: implemented from |
None |
Veber? Veber (GSK) filter: implemented from |
0.0 |
Egan? Egan (Pharmacia) filter: implemented from |
0.0 |
Muegge? Muegge (Bayer) filter: implemented from |
2.0 |
Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat |
0.55 |
PAINS? Pan Assay Interference Structures: implemented from |
0.0 alert |
Brenk? Structural Alert: implemented from |
0.0 alert: heavy_metal |
Leadlikeness? Leadlikeness: implemented from |
No; 1 violation:MW<1.0 |
Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) |
1.41 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
78% | at 5 - 20℃; for 3 h; | To a solution of compound 1 H-imidazole-2-carbaldehyde (5g, 52.08 mmol) in MeOH (50 mL) was added sodium borohydride (3.93g, 104.16 mmol) portion-wise, at 5 00, and the reaction mixture was allowed to stir at RT for 3h. The reaction mixture was quenched with brine (25 mL) and concentrated in vacuo. The crude compound was purified by silica gel column chromatography eluting with 10percent MeOH/CHCI3) to obtain (1H-imidazol-2-yl)-methanol as a pale yellow solid (4g, 78percent).R:0.1 (10percent MeOH/CHCI3).1H NMR (400MHz, CD3OD): O 6.97 (5, 2H), 4.61 (5, 2H). |
51% | With sodium tetrahydroborate In methanol at 20℃; for 1 h; Inert atmosphere | To a solution of 2-imidazolecarboxyaldehyde (18-1) (1.92 g, 20 mmol, 1.0 eq.) was suspended in methanol (30 ml), NaBH4 (1.52g, 40 mmol, 2.0 eq.) was added portion-wise. The reaction mixture was stirred at room temperature for 1 h under N2. It was quenched with 5 ml of brine. The solvent was removed and the solid was purified with silica gel column chromatography (DCM : MeOH = 20: 1) to afford 18-2 as a white solid. (1.0g, Yield: 51percent). |
51% | at 20℃; for 1 h; Inert atmosphere | Compound 26-2 (0449) To a solution of 2-imidazolecarboxyaldehyde (26-1) (1.92 g, 20 mmol, 1.0 eq) was suspended in methanol (30 mL), NaBH4 (1.52 g, 40 mmol, 2.0 eq) was added portion-wise. The reaction mixture was stirred at room temperature for 1 h under N2. It was quenched with 5 mL of brine. The solvent was removed and the solid was purified with silica gel column chromatography (DCM:MeOH=20:1) to afford a white solid. (1.0 g, Yield: 51percent). |
45.2% | With sodium tetrahydroborate In methanol; dichloromethane | Part A Preparation 2-hydroxymethyl-1H-imidazole 2-Imidazolecarboxyaldehyde (5.0 g, 52.0 mmol) was suspended in 200 mL of methanol. NaBH4 (3.95 g, 0.10 mol) was added portion-wise. The reaction mixture was stirred at room temperature for 1 h under N2. It was quenched with 10 mL of brine. The solvent was removed. The solid was washed with 5percent MeOH in CH2Cl2. The inorganic solid was filtered off. The filtrate was concentrated and chromatographed with 5percent MeOH in CH2Cl2 to give 2.32 g off-white solid (45.2percent yield). 1H NMR (DMSO-d6): δ 6.86 (s, 2H), 4.40 (s, 2H). |
A215005 [17334-08-6]
(1-Methyl-1H-imidazol-2-yl)methanol
Similarity: 0.90
A118970 [334893-99-1]
(5-Chloro-1-methyl-1H-imidazol-2-yl)methanol
Similarity: 0.73
A101376 [4856-97-7]
(1H-Benzoimidazol-2-yl)methanol
Similarity: 0.64
A207896 [1100750-16-0]
5,6,7,8-Tetrahydroimidazo[1,2-a]pyridin-6-ol
Similarity: 0.61