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| 171274-39-8 Chemical Structure| 171274-39-8

Structure of 171274-39-8

Chemical Structure| 171274-39-8

*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 [ 171274-39-8 ]

CAS No. :171274-39-8
Formula : C9H8Cl2O2
M.W : 219.06
SMILES Code : O=C(Cl)CC1=CC=C(Cl)C=C1OC
MDL No. :MFCD30489477

Safety of [ 171274-39-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 171274-39-8 ]

* 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 [ 171274-39-8 ]

[ 171274-39-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 170737-95-8 ]
  • [ 171274-39-8 ]
YieldReaction ConditionsOperation in experiment
6.5 g With thionyl chloride; at 60℃; 2-(4-Chloro-2-methoxyphenyl)acetic acid [CAS 170737-95-8] (5.8 g, 28.9 mmol) was added in small portions to thionyl chloride (50 ml_) and the resulting solution was stirred overnight at 60C. The solvent was concentrated under reduced pressure and co-evaporated with toluene to give 2-(4-chloro-2- methoxyphenyl)acetyl chloride 1a (6.5 g) as an oily residue that was used without further purification in the next step.
With sulfuryl dichloride; at 60℃; for 16h; 2-(4-Chloro-2-methoxyphenyl)acetic acid [CAS 170737-95-8] (5.8 g, 28.9 mmol) was added in small portions to thionyl chloride (50 mL) and the resulting solution was stirred overnight at 60C. The solvent was concentrated under reduced pressure and co-evaporated with toluene to give 2-(4-chloro-2-methoxyphenyl)- acetyl chloride 1a (6.5 g) as an oily residue that was used without further purification in the next step.
With oxalyl dichloride; N,N-dimethyl-formamide; In tetrahydrofuran; at 0 - 20℃; for 0.5h; Synthesis of intermediate 1a: A solution of <strong>[170737-95-8]2-(4-chloro-2-methoxyphenyl)acetic acid</strong> [CAS 170737-95-8] (20 g, 101 mmol) in dry THF (300 ml_) was cooled at 0C. Oxalyl chloride (18 ml_, 202 mmol) and two drops of DMF were added. The reaction mixture was stirred at room temperature for 30 min. The solvent was evaporated under reduced pressure. The residue was dissolved in ethanol (300 ml_) and the reaction mixture was stirred at room temperature for 1 h. The reaction mixture was concentrated under reduced pressure to give ethyl 2-(4-chloro-2- methoxyphenyl)acetate 1a (23 g), which was used in the next step without further purification.
6.5 g With thionyl chloride; at 60℃; 2-(4-Chloro-2-methoxyphenyl)acetic acid [CAS 170737-95-8] (5.8 g, 28.9 mmol) was added in small portions to thionyl chloride (50 mL) and the resulting solution was stirred overnight at 6000. The solvent was concentrated under reducedpressure and co-evaporated with toluene to give 2-(4-chloro-2-methoxyphenyl)- acetyl chloride 9a’ (6.5 g) as an oily residue that was used without furtherpurification in the next step.
With thionyl chloride; at 60℃; 2-(4-Chloro-2-methoxyphenyl)acetic acid [CAS 170737-95-8] (5.8 g, 28.9 mmol) was added in small portions to thionyl chloride (50 mL) and the resulting solutionwas stirred overnight at 6000. The solvent was concentrated under reduced pressure and co-evaporated with toluene to give 2-(4-chloro-2-methoxyphenyl)- acetyl chloride 9a’ (6.5 g) as an oily residue that was used without further purification in the next step.

  • 2
  • [ 171274-39-8 ]
  • [ 1082041-52-8 ]
  • 2-(4-chloro-2-methoxyphenyl)-1-(5-fluoro-7-methyl-1H-indol-3-yl)ethanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
2.03 g (0262) Diethylaluminum chloride 1 M in hexane (15.0 mL, 15.0 mmol) was added dropwise at 0C to a solution of 5-fluoro-7-methyl-1 H-indole [CAS 1082041 -52- 8] (1 .49 g, 10.0 mmol) in CH2CI2 (20 mL). After 30 min at 0C, a solution of 2- (4-chloro-2-methoxyphenyl)acetyl chloride 1a (3.28 g, 15.0 mmol, synthesis: see Example 1 ) in CH2CI2 (10 mL) was added slowly at 0C. The reaction was stirred at 0C for 3 h. 1 M Rochelle salt solution was added and the reaction mixture was stirred at room temperature for 30 min. The formed solids were filtered off and partitioned between EtOAc and 1 N HCI. The phases were separated. The aqueous layer was extracted with EtOAc. The organic phases were combined, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give 2-(4-chloro-2-methoxyphenyl)-1 - (5-fluoro-7-methyl-1 H-indol-3-yl)ethanone 8a (2.03 g).
 

Historical Records

Technical Information

Categories