Home Cart Sign in  
Chemical Structure| 88537-32-0 Chemical Structure| 88537-32-0

Structure of 88537-32-0

Chemical Structure| 88537-32-0

*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 [ 88537-32-0 ]

CAS No. :88537-32-0
Formula : C8H5NS2
M.W : 179.26
SMILES Code : C1(C=CS2)=C2C3=C(C=CS3)N1
MDL No. :MFCD13178401
InChI Key :VBSAGAKIMFPMFV-UHFFFAOYSA-N
Pubchem ID :13122712

Safety of [ 88537-32-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P264-P270-P280-P301+P312+P330-P305+P351+P338-P337+P313-P501

Application In Synthesis of [ 88537-32-0 ]

* 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 [ 88537-32-0 ]

[ 88537-32-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 88537-32-0 ]
  • [ 57103-20-5 ]
  • 4,4'-(9-phenyl-9H-carbazole-3,6-diyl)bis(4H-dithieno[3,2-b:2',3'-d]pyrrole) [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In o-xylene; toluene; at 160℃; for 48h; Pd2 (dba) 3 357.3 mg (0.39 mmol) and t-Bu3P mg 157.9 (0.78 mmol) of o-xylene dissolved in 50 ml after 10 minutes at room temperature in agitation. 4H-dithiol in no [3,2-b: 2 ', 3'-d] pyrrole 8.23 g (46 mmol), 3,6 - dibromo -9-phenyl-9H-carbazole 7.98 g (20 mmol) It was added, and t-BuONa 2.25 g (23.41 mmol) and reflux was stirred for 48hours at 160°C. Cold distilled water was added to 20 ml After completion of the reaction and extracted with ethyl acetate. The solvent was evaporated and dried over magnesium sulfate and filtered. After the compound was purified by column chromatography through 135 4,4 '- (9-phenyl -9H- carbazole-3,6-diyl) bis (4H- the furnace dithiane [3,2-b: 2', 3'-d ] pyrrole) to give 9.55 g (80percent yield).
66% With palladium diacetate; tris-(o-tolyl)phosphine; sodium t-butanolate; In toluene; Afterward, the Intermediate E and Intermediate D were used to perform Buchwald-Hartwig cross-coupling to synthesize 3.65 g (66percent) of Compound 109.
 

Historical Records

Technical Information

Categories