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1427358-97-1

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1427358-97-1 Usage

Explanation

The compound consists of 4 carbon atoms, 10 hydrogen atoms, 2 nitrogen atoms, 2 oxygen atoms, 1 sulfur atom, and 1 hydrochloride ion (HCl).

Explanation

The compound has a 7-membered ring structure with a spiro-fused linkage, which means two rings are connected by sharing a common atom.

Explanation

The compound contains a sulfur and nitrogen heterocycle, which is a ring structure with non-carbon atoms (sulfur and nitrogen) in the ring.

Explanation

The compound is formed by the reaction of 1-Thia-6-aza-spiro[3.3]heptane-1,1-dioxide with hydrochloric acid (HCl), making it a hydrochloride salt.

Explanation

1-Thia-6-aza-spiro[3.3]heptane-1,1-dioxide hydrochloride is used as an intermediate in the synthesis of various drugs.

Explanation

Due to its unique structural features and potential biological activities, the compound may have applications in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1427358-97-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,3,5 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1427358-97:
(9*1)+(8*4)+(7*2)+(6*7)+(5*3)+(4*5)+(3*8)+(2*9)+(1*7)=181
181 % 10 = 1
So 1427358-97-1 is a valid CAS Registry Number.

1427358-97-1Downstream Products

1427358-97-1Relevant articles and documents

TETRAHYDRO-IMIDAZO QUINOLINE COMPOSITIONS AS CBP/P300 INHIBITORS

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Paragraph 00137, (2019/04/11)

The present disclosure is directed to inhibitors of the CBP/p300 family of bromodomains. The compounds can be useful in the treatment of disease or disorders associated with the inhibition of the CBP/p300 family of bromodomains. For instance, the disclosure is concerned with compounds and compositions for inhibition of the CBP/p300 family of bromodomains, methods of treating, preventing, or ameliorating diseases or disorders associated with the inhibition of CBP/p300 family of bromodomains, and methods of synthesis of these compounds.

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