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Identification
CAS Number
4124-41-8
Name
4-Methylbenzenesulfonic Anhydride
Synonyms
1,3-bis(4-methylphenyl)-1,1,3,3-tetraoxo-1λ~6~,3λ~6~-dithioxane223-926-94-Toluenesulfonic anhydrideMFCD00008548p-Toluenesulfonic Anhydridep-tolylsulfonyl 4-methylbenzenesulfonate(4-methylphenyl)sulfonyl 4-methylbenzenesulfonate4-methyl benzenesulfonic anhydride4-methylbenzenesulfonic anhydride4-Methylbenzenesulfonic anhydride; Tosic anhydride4-Methylbenzenesulfonicanhydride4-methylbenzenesulfonyl 4-methylbenzene-1-sulfonate4-METHYLBENZENESULFONYL 4-METHYLBENZENESULFONATE4-Methylbenzenesulphonic anhydride, Tosic anhydride4-Methylbenzenesulphonic anhydride; Tosic anhydride4-Toluenesulfonic acid anhydride4-Toluenesulphonic anhydrideBenzenesulfonic acid, 4-methyl-, anhydridep-methylbenzenesulfonyl (tosylate)p-Toluene sulfonic anhydridep-Toluenesulfonicanhydridep-toluenesulfonicanhydride(rs20007372)p-Toluenesulphonic anhydrideP-TolueneSulphonicAnhydridep-toluenesulfonic anhydridetoluene-4-sulfonic anhydrideToluene-4-sulphonic anhydridetoluene-p-sulphonic anhydrideTosic anhydride
SMILES
Cc1ccc(S(=O)(=O)OS(=O)(=O)c2ccc(C)cc2)cc1
StdInChI
InChI=1S/C14H14O5S2/c1-11-3-7-13(8-4-11)20(15,16)19-21(17,18)14-9-5-12(2)6-10-14/h3-10H,1-2H3
StdInChIKey
PDVFSPNIEOYOQL-UHFFFAOYSA-N
Molecular Formula
C14H14O5S2
Molecular Weight
326.381
EINECS
223-926-9
MDL Number
MFCD00008548
Properties
Appearance
Off-white solid
Melting Point
118°C ~128°C
Safety Data
Symbol
GHS05
Signal Word
Danger
Hazard statements
H314
Precautionary Statements
P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
RIDADR
NONH for all modes of transport
WGK Germany
3
Specifications and Other Information of Our 4-Methylbenzenesulfonic Anhydride CAS 4124-41-8
Identification Methods
HNMR, HPLC
Purity
98% min
Shelf Life
2 years
Storage
Store at room temperature, in container tightly sealed; Protect from light. Store in a dry place at 16° for a long time. The product is easy to absorb moisture and needs to be stored with desiccant.
Known Application
- Organic synthesis - strong dehydration condensation agentEsterification reaction Activate carboxyl to accelerate ester formationPeptide bond formation Mildly catalyze amino acid condensationSulfonylation protecting group Introduce -SO₂Tol group to protect amino/hydroxyl groups
- Synthesis of pharmaceutical intermediatesAntiviral drugs, synthesis of acyclovir side chain Reaction yield increased >15%(compared with methanesulfonyl chloride method)Antitumor drugs, construction of temozolomide pyrimidine ring Avoid the use of highly toxic phosgeneAntibiotics, modification of β-lactam ring C3 position Selectivity >90%(such as cefixime precursor)
- Polymer material modificationPolyester catalyst Replacement of antimony oxide (reducing heavy metals) Material transmittance ↑8%, melting point stability improvedEpoxy resin curing accelerator Activate curing reaction at low temperature (60℃) Curing time shortened 40%Ionic liquid synthesis Preparation of sulfonic acid ionic liquid Conductivity ≥15 mS/cm (fuel cell electrolyte)
Key reaction characteristics
- Reaction activity is higher than p-toluenesulfonyl chloride, shortening the reaction time
- Selectivity, preferentially reacting with primary alcohols/primary amines to reduce secondary group side reactions
- Byproduct, water-soluble toluenesulfonic acid is generated, which is easy to separate and purify
- Stability, needs to be stored in a dry and sealed state (decomposed in water), and operation requires strict humidity control
General View of Documents
HNMR of 4-Methylbenzenesulfonic Anhydride CAS 4124-41-8
Links
This product is developed by our R&D company Warshel Chemical Ltd (https://www.warshel.com/).
Quick Inquiry
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