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1-(p-Carboxyphenyl)-prop-2-in-1-ol, also known as 1-(4-carboxyphenyl)-2-propanol, is an organic compound with the molecular formula C10H12O3. It is a colorless to pale yellow crystalline solid that is soluble in water and various organic solvents. 1-(p-Carboxyphenyl)-prop-2-in-1-ol is characterized by the presence of a carboxylic acid group (-COOH) attached to a phenyl ring, which is further connected to a propanol chain. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can undergo a range of chemical reactions, making it a versatile building block in organic chemistry.

1595-68-2

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1595-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1595-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1595-68:
(6*1)+(5*5)+(4*9)+(3*5)+(2*6)+(1*8)=102
102 % 10 = 2
So 1595-68-2 is a valid CAS Registry Number.

1595-68-2Relevant academic research and scientific papers

A highly selective FRET-based fluorescent probe for detection of cysteine and homocysteine

Shiu, Hoi-Yan,Chong, Hiu-Chi,Leung, Yun-Chung,Wong, Man-Kin,Che, Chi-Ming

supporting information; scheme or table, p. 3308 - 3313 (2010/06/19)

Fluorescent probe: A turn-on FRET-based fluorescent probe for selective detection of cysteine (Cys) and homocysteine (Hey) under physiological conditions was synthesised (see figure). The probe features excellent selectivity, fast response times and good linearity towards Cys and Hey detection

Electron-deficient alkynes as cleavable reagents for the modification of cysteine-containlng peptides in aqueous medium

Shiu, Hoi-Yan,Chan, Tak-Chung,Ho, Chi-Ming,Liu, Yungen,Wong, Man-Kin,Che, Chi-Ming

supporting information; experimental part, p. 3839 - 3850 (2009/12/31)

An efficient method has been developed for the chemoselective cysteine modification of unprotected peptides and proteins in aqueous media through the formation of a vinyl sulfide linkage by using electron-deficient alkynes, including alkynoic amides, esters and alkynones. The terminal alkynone-modified peptides could be converted back into the unmodified peptides (81 % isolated yield) by adding thiols under mild conditions. The usefulness of this thiol-assisted cleavage of the vinyl sulfide linkage in peptides has been exemplified by the enrichment of a cysteine-containing peptide (71% recovery) from a mixture of cysteine-containing and non-cysteine-containing peptides.

4- AND 5-ALKYNYLOXINDOLES AND 4- AND 5-ALKENYLOXINDOLES

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Page/Page column 11; 21, (2010/02/04)

4- and 5-alkynyloxindoles as well as 4- and 5-alkenyloxindoles having formula (I) and (II), wherein R, R, R, R, R, X and z have the meaning indicated in the specification, inhibit or modulate protein kinases, in particular JNK protein kinases and are useful as anti-inflammatory agents, particularly in the treatment of rheumatoid arthritis.

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