2-(Tetrahydropyran-2-yl)acetic Acid
95%
- Product Code: 241153
CAS:
13103-40-7
| Molecular Weight: | 144.17 g./mol | Molecular Formula: | C₇H₁₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03990565 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8ºC |
Product Description:
Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its main role is as a protected form of acetic acid, where the tetrahydropyranyl (THP) group acts as a protecting group for the carboxylic acid functionality. This protection allows selective reactions to occur at other reactive sites in complex molecule synthesis without interference from the acidic proton. It is particularly useful in multi-step syntheses of natural products and bioactive molecules where controlled deprotection is required under mild acidic conditions. The compound also finds use in the preparation of esters and amides through standard coupling reactions, after deprotection or while still protected, depending on the synthetic strategy.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿2,070.00 |
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| 5.000 G | 10-20 days | ฿21,980.00 |
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| 1.000 G | 10-20 days | ฿5,190.00 |
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2-(Tetrahydropyran-2-yl)acetic Acid
Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its main role is as a protected form of acetic acid, where the tetrahydropyranyl (THP) group acts as a protecting group for the carboxylic acid functionality. This protection allows selective reactions to occur at other reactive sites in complex molecule synthesis without interference from the acidic proton. It is particularly useful in multi-step syntheses of natural products and bioactive molecules where controlled deprotection is required under mild acidic conditions. The compound also finds use in the preparation of esters and amides through standard coupling reactions, after deprotection or while still protected, depending on the synthetic strategy.
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