Home Cart Sign in  
Chemical Structure| 612-40-8 Chemical Structure| 612-40-8

Structure of 612-40-8

Chemical Structure| 612-40-8

*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 [ 612-40-8 ]

CAS No. :612-40-8
Formula : C10H8O4
M.W : 192.17
SMILES Code : O=C(O)/C=C/C1=CC=CC=C1C(O)=O
MDL No. :MFCD00004380

Safety of [ 612-40-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 612-40-8 ]

* 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 [ 612-40-8 ]

[ 612-40-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 612-40-8 ]
  • [ 2848-01-3 ]
  • (2-carboxy-1-(2-carboxyphenyl)ethyl)(2-carboxyethyl)diphenylphosphonium chloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% With hydrogenchloride; In chloroform; water; at 80℃; for 10h; General procedure: Samples of tertiary phosphines and substituted cinnamic acids were dissolved in chloroform and 1 drop of concentrated hydrochloric acid solution was added. The reactions were carried out at a temperature of 80C in a water bath with a reverse refrigerator. Heated 10h. Upon completion of the reaction, the solvent was distilled in a Schott funnel. The precipitate was washed with diethyl ether and dried in vacuum.
 

Historical Records

Technical Information

Categories