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5-chloropyrazolo[1,5-a]pyrimidin-7-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

245095-96-9

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245095-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 245095-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 245095-96:
(8*2)+(7*4)+(6*5)+(5*0)+(4*9)+(3*5)+(2*9)+(1*6)=149
149 % 10 = 9
So 245095-96-9 is a valid CAS Registry Number.

245095-96-9SDS

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 5-Chloropyrazolo[1,5-a]pyrimidin-7-amine

1.2 Other means of identification

Product number -
Other names 7-AMINO-5-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE

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:245095-96-9 SDS

245095-96-9Downstream Products

245095-96-9Relevant academic research and scientific papers

Pyrazolo[1,5-a]pyrimidine with similar “amino-nitro-amino” arrangement characteristics to TATB: a novel heat-resistant explosive with fused structure

Yang, Feng,Xu, Yuangang,Wang, Pengcheng,Lin, Qiuhan,Bi, Fuqiang,Liu, Ning,Lu, Ming

, p. 2801 - 2808 (2021)

Exploring heat-resistant explosives that are easy to synthesize is a major challenge in the research of energetic materials. In this study, two novel fused-ring energetic compounds, namely 3,6-dinitropyrazolo[1,5-a]pyrimidine-5,7-diamine (4) and 5-amino-3,6-dinitropyrazolo[1,5-a]pyrimidin-7(4H)-one (5), were successfully preparedviaa simple synthetic method. In addition, their structure, thermal stability, mechanical sensitivity and detonation performance were fully explored. Noteworthily, compounds4and5both exhibit excellent thermal stability (TD(4) = 325 °C andTD(5) = 291 °C), particularly compound4, which features an “amino-nitro-amino” arrangement similar to that of TATB and exhibits a high density of 1.88 g cm?3and a greater thermal decomposition temperature than hexanitrostilbene (HNS, 316 °C). In addition, due to the aza-fused structure,4and5possess higher positive heats of formation (332.9 kJ mol?1and 181.4 kJ mol?1) than LLM-105 (11.0 kJ mol?1). These advanced features endow4and5with superior detonation performance (Vd(4) = 8338 m s?1andP(4) = 30.7 GPa;Vd(5) = 8097 m s?1andP(5) = 29.8 GPa) than TATB (Vd= 8179 m s?1andP= 30.5 GPa) and HNS (Vd= 7170 m s?1andP= 21.8 GPa). This study enriches prospects for the molecular design and crystal engineering of novel energetic materials with admirable molecular stability.

Pyrazolopyrimidines and related heterocycles as CK2 inhibitors

-

Page/Page column 59, (2016/05/02)

The invention provides compounds that inhibit protein kinase CK2 activity (CK2 activity), and compositions containing such compounds. These compounds and compositions are useful for treating proliferative disorders such as cancer, as well as other kinase-associated conditions including inflammation, pain, and certain immunological disorders, and have the following general formula:

Pyrazolopyrimidin CK2 and related heterocyclic compound as an inhibitor

-

Paragraph 0270, (2016/10/08)

The invention provides compounds that inhibit protein kinase CK2 activity (CK2 activity), and compositions containing such compounds. These compounds and compositions are useful for treating proliferative disorders such as cancer, as well as other kinase-associated conditions including inflammation, pain, and certain immunological disorders, and have the following general formula:

FUSED TRICYCLIC COMPOUNDS AS mTOR INHIBITORS

-

, (2013/03/26)

The present invention relates to certain pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidine and dipyrazolopyrimidine compounds of Formula (I) as inhibitors of mammalian Target Of Rapamycin (mTOR) kinase, which is also known as FRAP, RAFT, RAPT or SEP. The compounds

FUSED TRICYCLIC INHIBITORS OF MAMMALIAN TARGET OF RAPAMYCIN

-

, (2012/03/26)

This invention relates to novel fused tricyclic compounds that are inhibitors of mammalian Target of Rapamycin (mTOR) kinase, which is also known as FRAP, RAFT, RAPT or SEP, and are useful in the treatment of cellular proliferative diseases, for example c

FUSED TRICYCLIC INHIBITORS OF MAMMALIAN TARGET OF RAPAMYCIN

-

, (2012/04/23)

This invention relates to novel fused tricyclic compounds that are inhibitors of mammalian Target of Rapamycin (mTOR) kinase which is also known as FRAP, RAFT, RAPT or SEP, and are useful in the treatment of cellular proliferative diseases for example can

FUSED TRICYCLIC INHIBITORS OF MAMMALIAN TARGET OF RAPAMYCIN

-

, (2012/04/23)

This invention relates to novel fused tricyclic compounds that are inhibitors of mammalian Target of Rapamycin (mTOR) kinase, which is also known as FRAP, RAFT, RAPT or SEP, and are useful in the treatment of cellular proliferative diseases, for example c

FUSED TRICYCLIC INHIBITORS OF MAMMALIAN TARGET OF RAPAMYCIN

-

, (2012/03/26)

This invention relates to novel fused tricyclic compounds that are inhibitors of mammalian Target of Rapamycin (mTOR) kinase, which is also known as FRAP, RAFT, RAPT or SEP, and are useful in the treatment of cellular proliferative diseases, for example c

FUSED TRICYCLIC COMPOUNDS AS NOVEL mTOR INHIBITORS

-

, (2011/02/24)

The present invention provides Fused Tricyclic Compounds of the Formula (I) wherein Q, R1, R2, R3, and R4 are as defined herein, and pharmaceutically acceptable salts of such Fused Tricyclic Compounds. The Fused Tricyclic Compounds are useful in the treatment of cancer and other proliferative disorders.

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