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2,4-dichloro-7-(2-trimethylsilanyl-ethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid is a complex chemical compound characterized by the presence of dichloro, pyrrolo, and pyrimidine groups. It is a carboxylic acid derivative featuring a trimethylsilanyl-ethoxymethyl substituent, which may contribute to its unique properties and potential applications in various fields.

950661-85-5

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950661-85-5 Usage

Uses

Given the lack of specific information on the uses of 2,4-dichloro-7-(2-trimethylsilanyl-ethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid, its potential applications can be inferred based on its structural features and the common uses of similar compounds. Here are some possible applications across different industries:
Used in Pharmaceutical Industry:
2,4-dichloro-7-(2-trimethylsilanyl-ethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid may be used as a pharmaceutical intermediate or a lead compound for the development of new drugs. Its carboxylic acid and pyrimidine core could be exploited for the synthesis of bioactive molecules with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dichloro-7-(2-trimethylsilanyl-ethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid could be utilized as a precursor for the synthesis of agrochemicals, such as herbicides, insecticides, or fungicides. The dichloro and pyrrolo-pyrimidine groups may provide the necessary structural features for the development of compounds with pesticidal properties.
Used in Materials Science:
2,4-dichloro-7-(2-trimethylsilanyl-ethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid may also find applications in materials science, particularly in the development of new materials with unique properties. The presence of the trimethylsilanyl-ethoxymethyl substituent could contribute to the compound's compatibility with various polymers or other materials, enabling its use in the synthesis of novel composites or coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 950661-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,6,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 950661-85:
(8*9)+(7*5)+(6*0)+(5*6)+(4*6)+(3*1)+(2*8)+(1*5)=185
185 % 10 = 5
So 950661-85-5 is a valid CAS Registry Number.

950661-85-5Upstream product

950661-85-5Relevant academic research and scientific papers

PYRROLOPYRIMIDINE DERIVATIVES USED AS HSP90 INHIBITORS

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Page/Page column 39-40, (2008/06/13)

Compounds of formula (I) have HSP90 inhibitory activity and are therefore useful in the treatment of, inter alia, cancer: Formula (I) wherein Ri is hydrogen, fluoro, chloro, bromo, or a radical of formula -X-Alk1-(Z)m-(Alk2)n-Q wherein X is -O-, -S- -S(O)-, -SO2-, or -NH-, Z is -O-, -S-, -(C=O)-, -(C=S)-, -S(O)-, -SO2-, -NRA-, or, in either orientation -C(=O)O-, -C(=O)NRA- , -C(=S)NRA-, -SO2NRA-, -NRAC(=O)-, or -NRASO2- wherein RA is hydrogen or C1-C6 alkyl AIk1 and AIk2 are optionally substituted divalent C1-C3 alkylene or C2-C3 alkenylene radicals, m, n and p are independently 0 or 1 , and Q is hydrogen or an optionally substituted carbocyclic or heterocyclic radical; R2 is a radical of formula -(Ar1)p-(Alk1)q-(Z)r-(Alk2)s-Q wherein Ar1 is an optionally substituted aryl or heteroaryl radical, Alk1, Alk2, Z, and Q are as defined above, and p, q, r and s are independently 0 or 1 ; and R3 is cyano (-CN), fluoro, chloro, bromo, methyl in which in which one or more hydrogen atoms are optionally replaced by fluorine atoms, ethyl in which in which one or more hydrogen atoms are optionally replaced by fluorine atoms, cyclopropyl, -OH, -CH2OH, -C(O)NH2, -C(O)CH3, Or -NH2.

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