Home Cart Sign in  
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| 132794-08-2 Chemical Structure| 132794-08-2

Structure of 132794-08-2

Chemical Structure| 132794-08-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

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

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 132794-08-2 ]

CAS No. :132794-08-2
Formula : C7H2Cl2F2O
M.W : 210.99
SMILES Code : O=C(Cl)C1=CC(F)=C(Cl)C=C1F
MDL No. :MFCD00236600

Safety of [ 132794-08-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P305+P351+P338-P405-P260-P310-P363-P264-P303+P361+P353-P280-P304+P340-P301+P330+P331-P321
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 132794-08-2 ]

* 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 [ 132794-08-2 ]

[ 132794-08-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 132794-07-1 ]
  • [ 132794-08-2 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; EXAMPLE 3 Preparation of 4-chloro-2,5-difluorobenzoyl Chloride 38.5 g <strong>[132794-07-1]4-chloro-2,5-difluorobenzoic acid</strong> (0.2 mole) was placed in a 250 mL, 3-necked roundbottom flask equipped with a magnetic stirbar, a thermometer, and a water-cooled condenser. 238 g thionyl chloride was added in one lot. The mixture was stirred and heated on a water bath. At about 58-60 C. the solid dissolved with evolution of gas and formation of foam. The mixture was stirred and maintained at 60 C. until all the solid dissolved - about 30 minutes. It was then heated in a boiling water bath to reflux and held there for 2 hours. The excess thionyl chloride was distilled out. The contents were cooled and then distilled under reduced pressure. The capillary GC analysis showed the distilled product to be 99.6% pure. The yield was 41.1 g, 98%.
With thionyl chloride; In N,N-dimethyl-formamide; at 70 - 80℃; for 2.5h; After stirring a mixture of <strong>[132794-07-1]4-chloro-2,5-difluorobenzoic acid</strong>, thionyl chloride and DMF at 70C for one hour and additionally at 80C for 1.5 hours, the solvent was removed under reduced pressure and THF was added. , This reaction solution was added to a mixture of methyl 3-aminothiophene-2-carboxylate, THF and diisopropylethylamine in an MeOH-ice bath and stirred at room temperature for 1.5 days to give methyl 3-[(4-chloro-2,5-difluorobenzoyl)amino]thiophene-2-carboxylate.
With thionyl chloride; In N,N-dimethyl-formamide; at 80℃; General procedure: A mixture of 4-bromo-2,5-difluorobenzoic acid (11a, 53.28 g), thionyl chloride (165 mL) and DMF (0.87 mL) was stirred at 80 C for 1.5 h, and cooled down to room temperature. The mixture was evaporated in vacuo, and the resulting residue was dissolved in chloroform (300 mL). To the solution was added dropwise 28 wt % aqueous ammonia (300 mL) at 5 C, and the mixture was stirred at 5 C for 0.5 h. The mixture was extracted with chloroform, and the organic layer was dried. The desiccant was removed by filtration and the filtrate was evaporated in vacuo to obtain a pale yellow solid. The mixture of the obtained solid and phosphoryl chloride (195 mL) was stirred at 80 C for 2 h, and cooled down to room temperature. The mixture was evaporated in vacuo, and the resulting residue was treated with diethyl ether (500 mL) and ice-water (300 mL), then stirred at room temperature for 0.5 h. The mixture was extracted with diethyl ether and the organic layer was washed with saturated aqueous sodium hydrogen carbonate and brine, and then dried. The desiccant was removed by filtration and the filtrate was evaporated in vacuo to obtain 9h (41.57 g, 85%) as a pale yellow solid.
  • 2
  • [ 132794-08-2 ]
  • [ 135748-35-5 ]
 

Historical Records

Technical Information

Categories