Home Cart Sign in  
Chemical Structure| 184970-30-7 Chemical Structure| 184970-30-7

Structure of 184970-30-7

Chemical Structure| 184970-30-7

*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 [ 184970-30-7 ]

CAS No. :184970-30-7
Formula : C8H8Cl2O
M.W : 191.05
SMILES Code : CC(O)C1=CC(Cl)=CC(Cl)=C1
MDL No. :MFCD11520973
InChI Key :URTUBSJCDSAWGE-UHFFFAOYSA-N
Pubchem ID :21744446

Safety of [ 184970-30-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 184970-30-7 ]

* 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 [ 184970-30-7 ]

[ 184970-30-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 184970-30-7 ]
  • [ 14401-72-0 ]
  • 2
  • [ 51-36-5 ]
  • [ 917-54-4 ]
  • [ 14401-72-0 ]
  • [ 184970-30-7 ]
  • 3
  • [ 14401-72-0 ]
  • [ 184970-30-7 ]
YieldReaction ConditionsOperation in experiment
100% With sodium tetrahydroborate; ethanol; for 0.0833333h; Toa solution of l -(3,5-dichlorophenyl)ethan-l-one (l .OOg, 5.29 mmol) in EtOH(10 mL) at room temperature was added solid NaB (100 mg, 2.64 mmol) in threeportions over 5 min with stirring. The solvent was evaporated and the resultantwhite solid treated with 1M HC1 (20 mL) and DCM (70 mL). The phases wereseparated and the organic phase was washed with brine (20 mL), dried (Na2S04),the mixture was filtered and the filtrate evaporated to dryness to afford(+/-)-l -(3,5-dichlorophenyl)ethan-l-ol as a cloudy oil (1025 mg, 100%) ; HNMR (250 MHz, CDC13) delta 1.47 (d, 3H), 4.85 (q, 1H), 7.24 - 7.28 (m,3H)
 

Historical Records

Technical Information

Categories