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1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois a chemical compound with the molecular formula C6H5BrN6. It is a derivative of pyrazolo[3,4-d]pyrimidine and contains a bromine atom at the 3-position. 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois known for its potent antiproliferative and anti-inflammatory activities, making it a valuable asset in medicinal chemistry and drug development. Its unique structure and pharmacological properties have garnered interest among researchers for its potential therapeutic applications in treating cancer and autoimmune diseases.

144750-82-3

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144750-82-3 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois used as a key intermediate in the synthesis of various pharmaceutical compounds for its potent antiproliferative and anti-inflammatory properties. Its ability to inhibit the proliferation of cancer cells and reduce inflammation makes it a promising candidate for the development of novel therapeutic agents.
Used in Cancer Treatment:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois used as an anticancer agent for its potential to target and inhibit the growth of cancer cells. Its antiproliferative activity allows it to disrupt the cell cycle and induce apoptosis in cancer cells, making it a valuable tool in the fight against various types of cancer.
Used in Autoimmune Disease Treatment:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois used as a potential therapeutic agent for the treatment of autoimmune diseases due to its anti-inflammatory properties. Its ability to modulate the immune system and reduce inflammation can help alleviate the symptoms and progression of autoimmune disorders.
Used in Drug Development Research:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromois used as a valuable research tool for the development of novel therapies for various diseases. Its unique structure and pharmacological properties provide insights into the design and synthesis of new drugs with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 144750-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,5 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144750-82:
(8*1)+(7*4)+(6*4)+(5*7)+(4*5)+(3*0)+(2*8)+(1*2)=133
133 % 10 = 3
So 144750-82-3 is a valid CAS Registry Number.

144750-82-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-bromo-

1.2 Other means of identification

Product number -
Other names 3-BROMO-1H-PYRAZOLO[3,4-B]PYRAZINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:144750-82-3 SDS

144750-82-3Relevant academic research and scientific papers

Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: Synthesis, deamination and tautomerism

Seela, Frank,Xu, Kuiying

, p. 3034 - 3045 (2007)

The syntheses and properties of 8-aza-7-deazapurine (pyrazolo[3,4-d] pyrimidine) ribonucleosides related to 2-aminoadenosine and isoguanosine are described. Glycosylation of 8-aza-7-deazapurine-2,6-diamine 5 with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-d-ribofur

PYRROLOTRIAZINONE DERIVATIVES AS PI3K INHIBITORS

-

Page/Page column 96, (2014/05/07)

New pyrrolotriazinone derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Phosphoinositide 3-Kinases (PI3Ks).

Real-time linear detection probes: sensitive 5'-minor groove binder-containing probes for PCR analysis

-

, (2008/06/13)

Oligonucleotide probes/conjugates are provided along with method for their use in assays to monitor amplification wherein the signal produced does not rely on 5′ nuclease digestion.

Synthesis of pyrazolo 3,4-d pyrimidine analogues of the potent agent N-4-2-2-amino-4 3H-oxo-7H-pyrrolo 2,3-d pyrimidin-5-yl ethylbenzoyl-L-glutamic acid (LY231514)

Taylor, Edward C.,Patel, Hemantkumar H.

, p. 8089 - 8100 (2007/10/02)

Several pyrazolo[3,4-d]pyrimidine analogues of the potent antitumor agent N-{4-[2-(2-amino-4(3 H)-oxo-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl}-L-glutamic acid (LY231514, 5) have been prepared. A principal synthetic step proved to be a palladium-cata

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