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4-Fluoro-3-iodobenzoic+acid


143,203  results were found

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Catalog Number: (102839-368)

Supplier:  Matrix Scientific
Description:   Methyl-2-iodo-3-nitrobenzoate ≥97%
Catalog Number: (76942-700)

Supplier:  AOB CHEM USA
Description:   Methyl-4-iodo-3-nitrobenzoate ≥97%
Supplier:  AMBEED, INC
Description:   Methyl-2-iodo-5-nitrobenzoate 98%
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 006684-25G , MDL Number: MFCD00270107
Catalog Number: (77292-980)

Supplier:  AMBEED, INC
Description:   4-Iodobenzhydrazide 95%
Supplier:  TCI America
Description:   CAS Number: 5326-47-6
MDL Number: MFCD00007849
Molecular Formula: C7H6INO2
Molecular Weight: 263.03
Purity/Analysis Method: >98.0% (T)
Form: Crystal
MSDS SDS
Supplier:  AMBEED, INC
Description:   (S)-2-(2-(Benzylamino)-3-phenylpropanamido)-5-iodobenzoic acid, Purity: 99%, CAS Number: 1594094-64-0, Appearance: White to Pale-yellow to Yellow-brown Solid, Storage: Keep in dark place, Inert atmosphere, Store in freezer, under -20 deg C, Size: 10mg
Supplier:  AMBEED, INC
Description:   Methyl-4-iodo-3-nitrobenzoate 98%
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 006682-5G , MDL Number: MFCD00025114
Supplier:  BeanTown Chemical
Description:   CAS: 18179-39-0; MDL No: MFCD06797864 Solid; Molecular Formula: C8H7IO3; MW: 278.05 Melting Point: 69-73° Light Sensitive
MSDS SDS
Supplier:  Bachem Americas
Description:   The Wang support, p-benzyloxybenzyl alcohol resin, is the most widely used resin for attaching carboxylic acids for further functionalization. Cleavage conditions for the ester anchor involve concentrated TFA or TFA/CHâ‚‚Clâ‚‚ to provide carboxylic acids or cyclization-cleavage under acidic or basic conditions. Release of an amide function by treatment with an amine in the presence of a Lewis acid was also reported. Wang resin was used to add vinyl and iodobenzoic acids via carbodiimide coupling and the products subjected to Heck conditions with alkenes or with alkynes or to Suzuki coupling with boron reagents. The Ugi multicomponent condensation reaction was conducted on Wang resin with the carboxylic acid, amine or isonitrile as the anchored functional group. Solid-phase lactam syntheses were also achieved by reaction of the resin-bound isonitrile with an amine and an ω-keto-acid as well as other synthetic transformations such as the Biginelli reaction and construction of heterocycles such as quinolones, imidazoles, hydantoins, and 1,4-benzodiazepine-2,5-diones. On a Wang resin primary, secondary, and tertiary alcohols have been converted to 4-methoxybenzyl ethers. As well as anchoring carboxylic acids to Wang resin, phenols were attached under Mitsunobu conditions, subjected to further transformations and cleaved under acidic conditions.
Supplier:  AMBEED, INC
Description:   Ethyl 5-chloro-2-iodobenzoate 95%
Supplier:  AMBEED, INC
Description:   Benzyl-4-iodobenzoate 95%
Supplier:  AOB CHEM USA
Description:   3-Iodobenzo[b]thiophene ≥97%
Supplier:  AMBEED, INC
Description:   Methyl-4-hydroxy-3-iodobenzoate 97%
Supplier:  AOB CHEM USA
Description:   2-Iodobenzo[b]thiophene ≥97%
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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