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Benzaldehyde, 4-hydroxy-2-iodo-, also known as 2-iodo-4-hydroxybenzaldehyde, is an organic compound with the molecular formula C7H5IO2. It features a benzene ring with a hydroxyl group and an iodine atom attached to it. Known for its characteristic almond-like odor, Benzaldehyde, 4-hydroxy-2-iodo- is commonly used as a reagent in organic synthesis and has potential applications in the production of pharmaceuticals, fragrances, and other chemical compounds. Furthermore, it has been studied for its potential antimicrobial and antifungal properties.

90151-01-2

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90151-01-2 Usage

Uses

Used in Organic Synthesis:
Benzaldehyde, 4-hydroxy-2-iodois used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Benzaldehyde, 4-hydroxy-2-iodois used as an intermediate in the synthesis of various drugs. Its presence in the molecular structure can contribute to the biological activity of the final product, enhancing the therapeutic effects of the medication.
Used in Fragrance Industry:
Due to its almond-like odor, Benzaldehyde, 4-hydroxy-2-iodois used as a fragrance ingredient in the perfumery and cosmetics industry. It can be incorporated into various formulations to provide a pleasant and distinctive scent.
Used in Antimicrobial and Antifungal Applications:
Benzaldehyde, 4-hydroxy-2-iodohas been studied for its potential antimicrobial and antifungal properties. It can be used as an active ingredient in disinfectants, sanitizers, and preservatives to inhibit the growth of harmful microorganisms and maintain the safety and quality of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 90151-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90151-01:
(7*9)+(6*0)+(5*1)+(4*5)+(3*1)+(2*0)+(1*1)=92
92 % 10 = 2
So 90151-01-2 is a valid CAS Registry Number.

90151-01-2Relevant articles and documents

INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE - SYNTHESIS AND USE THEREOF FOR TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA AND LYMPHOMA

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Page/Page column 23, (2021/05/07)

The present invention relates to new compounds of general formula I, their synthesis, their pharmaceutically acceptable salts, and their use in treatment of T-cell acute lymphoblastic leukemia and lymphoma.

A bright two-photon fluorescent probe for real-time monitoring autophagy in living cells

Jiang, Chuankun,Li, Longchun,Jiang, Jiacheng,Hou, Lilin,Fang, Gemin,Haizhu, Yu,Meng, Xiangming

supporting information, p. 447 - 450 (2019/08/07)

A novel donor-acceptor (D-A) type of two-photon (TP) fluorescent probe, i.e. Lyso-OSC, based on the lysosome-targeting morpholine group was developed. The polarity sensing coumarin group was functionalized as the acceptor and the 1-vinyl-4-methoxybenzene group was engineered as the donor. The fluorescence intensity and emission maximum wavelength of Lyso-OSC are highly sensitive to the polarity changes of solvent. The two-photon absorption cross-section and tissue penetration depth are up to 254 GM and 150 μm, respectively. The strong fluorescence, high sensitivity to polarity, low cytotoxicity, and accurate lysosome-targeting ability entail Lyso-OSC the excellent performance in detecting the polarity changes of cellular environment. To this end, a bright, real-time imaging autophagy of living cells has been achieved.

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