(R)-1-(4-iodophenyl)ethan-1-ol

95%

Reagent Code: #231309
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CAS Number 220089-24-7

science Other reagents with same CAS 220089-24-7

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. The iodine substituent allows for easy incorporation of radioactive iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) or single-photon emission computed tomography (SPECT). Its chiral center enables selective interactions in biological systems, enhancing the specificity of target molecules in drug design. Also employed in asymmetric synthesis to introduce chirality in more complex bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,940.00
250mg
10-20 days ฿15,800.00
1g
10-20 days ฿55,140.00
(R)-1-(4-iodophenyl)ethan-1-ol
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. The iodine substituent allows for easy incorporation of radioactive iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) or single-photon emission computed tomography (SPECT). Its chiral center enables selective interactions in biological systems, enhancing the specificity of target molecules in drug design. Also employ

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. The iodine substituent allows for easy incorporation of radioactive iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) or single-photon emission computed tomography (SPECT). Its chiral center enables selective interactions in biological systems, enhancing the specificity of target molecules in drug design. Also employed in asymmetric synthesis to introduce chirality in more complex bioactive molecules.

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