成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 2034-22-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 2034-22-2
Chemical Structure| 2034-22-2
Structure of 2034-22-2 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 2034-22-2 ]

Related Doc. of [ 2034-22-2 ]

Alternatived Products of [ 2034-22-2 ]
Product Citations

Product Details of [ 2034-22-2 ]

CAS No. :2034-22-2 MDL No. :MFCD00005184
Formula : C3HBr3N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JCGGPCDDFXIVQB-UHFFFAOYSA-N
M.W : 304.77 Pubchem ID :16253
Synonyms :

Calculated chemistry of [ 2034-22-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.69
TPSA : 28.68 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.48
Log Po/w (XLOGP3) : 3.14
Log Po/w (WLOGP) : 2.7
Log Po/w (MLOGP) : 1.64
Log Po/w (SILICOS-IT) : 3.34
Consensus Log Po/w : 2.46

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.17
Solubility : 0.0206 mg/ml ; 0.0000676 mol/l
Class : Moderately soluble
Log S (Ali) : -3.41
Solubility : 0.118 mg/ml ; 0.000387 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.78
Solubility : 0.0507 mg/ml ; 0.000166 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.26

Safety of [ 2034-22-2 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P273-P280-P301+P310+P330-P302+P352+P312-P304+P340+P311-P305+P351+P338-P332+P313-P337+P313-P403+P233-P405-P501 UN#:2811
Hazard Statements:H300-H311+H331-H315-H319-H335-H401 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2034-22-2 ]

* 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.

  • Downstream synthetic route of [ 2034-22-2 ]

[ 2034-22-2 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 2034-22-2 ]
  • CH3X [ No CAS ]
  • [ 1003-91-4 ]
  • 3
  • [ 2034-22-2 ]
  • [ 74-88-4 ]
  • [ 1003-91-4 ]
YieldReaction ConditionsOperation in experiment
94% Step 1. 2,4,5-Tribromo-l-methyl-lH-imidazole (0975) [00314] To a suspension of sodium hydride (0.787 g, 19.69 mmol) in DMF (15 mL) was added 2, 4, 5-tribromo-lH-imidazole (5 g, 16.41 mmol) in DMF (10 mL) at ambient temperature. The mixture was stirred at 50 °C for 1 h, cooled to 0 °C, and treated with methyl iodide (1.128 ml, 18.05 mmol). The mixture was warmed to 50 °C and stirred 16 h, the DMF was removed under reduced pressure and EtOAc was added. The mixture was washed with water, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (eluting with a gradient of 10-80percent EtOAc/hexanes) afforded 4.87 g (94percent) of 2,4,5-tribromo-l -methyl- lH-imidazole. 1H MR (300 MHz, CDC13) delta 3.62 (s, 3H). MS (ESI) m/z 316.77 [M+H]+.
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 2034-22-2 ]

Bromides

Chemical Structure| 1003-91-4

[ 1003-91-4 ]

2,4,5-Tribromo-1-methylimidazole

Similarity: 0.96

Chemical Structure| 16681-56-4

[ 16681-56-4 ]

2-Bromo-1H-imidazole

Similarity: 0.68

Chemical Structure| 2302-25-2

[ 2302-25-2 ]

4-Bromo-1H-imidazole

Similarity: 0.68

Chemical Structure| 16681-59-7

[ 16681-59-7 ]

2-Bromo-1-methyl-1H-imidazole

Similarity: 0.67

Chemical Structure| 25676-75-9

[ 25676-75-9 ]

4-Bromo-1-methylimidazole

Similarity: 0.67

Related Parent Nucleus of
[ 2034-22-2 ]

Imidazoles

Chemical Structure| 1003-91-4

[ 1003-91-4 ]

2,4,5-Tribromo-1-methylimidazole

Similarity: 0.96

Chemical Structure| 16681-56-4

[ 16681-56-4 ]

2-Bromo-1H-imidazole

Similarity: 0.68

Chemical Structure| 2302-25-2

[ 2302-25-2 ]

4-Bromo-1H-imidazole

Similarity: 0.68

Chemical Structure| 16681-59-7

[ 16681-59-7 ]

2-Bromo-1-methyl-1H-imidazole

Similarity: 0.67

Chemical Structure| 25676-75-9

[ 25676-75-9 ]

4-Bromo-1-methylimidazole

Similarity: 0.67

; ;