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1144080-27-2

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1144080-27-2 Usage

Description

Tert-butyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)hydrazinecarboxylate is a hydrazine derivative featuring a tert-butyl ester group and a carboxylate functional group. This complex and specific molecular structure suggests potential applications in organic synthesis and medicinal chemistry, as well as a possible role as a building block for more complex molecules and pharmaceuticals.

Uses

Used in Organic Synthesis:
Tert-butyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)hydrazinecarboxylate is used as a synthetic intermediate for the creation of various organic compounds due to its unique structure and potential reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, tert-butyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)hydrazinecarboxylate is used as a precursor in the development of pharmaceuticals, leveraging its specific molecular features to contribute to the design of new drugs.
Used in Pharmaceutical Development:
Tert-butyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)hydrazinecarboxylate is used as a building block in the synthesis of complex molecules and pharmaceuticals, potentially leading to the discovery of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1144080-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,4,0,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1144080-27:
(9*1)+(8*1)+(7*4)+(6*4)+(5*0)+(4*8)+(3*0)+(2*2)+(1*7)=112
112 % 10 = 2
So 1144080-27-2 is a valid CAS Registry Number.

1144080-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl 2-(1,4-dioxaspiro[4.5]dec-8-yl)hydrazinecarbo xylate

1.2 Other means of identification

Product number -
Other names Benzamide,N-(1,4-dihydro-4-oxo-2-quinazolinyl)

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:1144080-27-2 SDS

1144080-27-2Relevant articles and documents

PYRAZOLOPYRIMIDINE DERIVATIVES, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR USE IN PREVENTING OR TREATING CANCER, AUTOIMMUNE DISEASE AND BRAIN DISEASE CONTAINING THE SAME AS AN ACTIVE INGREDIENT

-

Paragraph 959-963, (2018/12/02)

The present invention relates to a pyrazolopyrimidine derivative, a preparation method thereof and a pharmaceutical composition comprising the same as an active ingredient for the prevention or treatment of cancer, autoimmune disease and brain disease. The pyrazolopyrimidine derivative of the present invention exhibits excellent Bruton's tyrosine kinase inhibition activity, so that it can be effectively used as a pharmaceutical composition for the prevention or treatment of cancer, autoimmune disease and Parkinson's disease.

Pyrazolopyrimidines as highly potent and selective, ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR): Optimization of the 1-substituent

Curran, Kevin J.,Verheijen, Jeroen C.,Kaplan, Joshua,Richard, David J.,Toral-Barza, Lourdes,Hollander, Irwin,Lucas, Judy,Ayral-Kaloustian, Semiramis,Yu, Ker,Zask, Arie

scheme or table, p. 1440 - 1444 (2010/07/06)

A series of pyrazolopyrimidine mammalian Target Of Rapamycin (mTOR) inhibitors with various substituents at the 1-position have been prepared, resulting in compounds with excellent potency, selectivity and microsomal stability. Combination of a 1-cyclohexyl ketal group with a 2,6-ethylene bridged morpholine in the 4-position and a ureidophenyl group in the 6-positon resulted in compound 8a, that selectively suppressed key mTOR biomarkers in vivo for at least 8 h following iv administration and showed excellent oral activity in a xenograft tumor model.

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