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Chemical Structure| 98-29-3 Chemical Structure| 98-29-3
Chemical Structure| 98-29-3

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4-tert-Butylcatechol (TBC) is an organic compound with antioxidant and polymerization-inhibiting properties. It is primarily used as a polymerization inhibitor and antioxidant.

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Product Details of 4-tert-Butylcatechol

CAS No. :98-29-3
Formula : C10H14O2
M.W : 166.22
SMILES Code : OC1=CC=C(C(C)(C)C)C=C1O
MDL No. :MFCD00002201
InChI Key :XESZUVZBAMCAEJ-UHFFFAOYSA-N
Pubchem ID :7381

Safety of 4-tert-Butylcatechol

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H318-H351-H410
Precautionary Statements:P201-P202-P264-P270-P273-P280-P301+P312+P330-P305+P351+P338+P310-P308+P313-P391-P405-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of 4-tert-Butylcatechol

* 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 [ 98-29-3 ]

[ 98-29-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 98-29-3 ]
  • [ 16657-10-6 ]
  • [ 104-15-4 ]
  • [ 16657-07-1 ]
YieldReaction ConditionsOperation in experiment
In toluene; Stage A: 4-bromo-3H-indene 30 g of 4-bromo-1-indanol is dissolved in 720 ml of toluene, 27 g of paratoluene sulphonic acid is added, then 0.93 g of 4-tertbutylcatechol is added. The mixture is taken to reflux for one hour. After cooling to 20 C., the organic phase is washed with 25 ml of N sodium hydroxide, dried and concentrated to dryness, and the residue is chromatographed on silica, eluding with a hexane-difluoro dichloro ethane mixture (95-5), and 24.6 g of expected product is isolated. Aromatic 1544 cm-1
  • 2
  • [ 51792-34-8 ]
  • [ 98-29-3 ]
  • 6-(tert-butyl)benzo[b]thieno[3,4-e][1,4]dioxine [ No CAS ]
 

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