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6,7-DIHYDRO-2''H,5H,5''H-SPIRO[1-BENZOTHIOPHENE-4,4''-IMIDAZOLIDINE]-2'',5''-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69300-50-1

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69300-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69300-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,0 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69300-50:
(7*6)+(6*9)+(5*3)+(4*0)+(3*0)+(2*5)+(1*0)=121
121 % 10 = 1
So 69300-50-1 is a valid CAS Registry Number.

69300-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[6,7-dihydro-5H-1-benzothiophene-4,5'-imidazolidine]-2',4'-dione

1.2 Other means of identification

Product number -
Other names -

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:69300-50-1 SDS

69300-50-1Downstream Products

69300-50-1Relevant academic research and scientific papers

Spiro tetrahydro-benzothiophen derivatives useful for the treatment of neurodegenerative diseases

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Paragraph 0138-0140, (2014/01/07)

The present invention provide compounds of Formula (I) used as BACE inhibitors for the treatment of neurodegenerative diseases.

SPIRO TETRAHYDRO - BENZOTHIOPHEN DERIVATIVES USEFUL FOR THE TREATMENT NEURODEGENERATIVE DISEASES

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Page/Page column 60, (2014/01/07)

The present invention provide compounds of Formula (I) used as BACE inhibitors for the treatment of neurodegenerative diseases

Spiro hydantoin aldose reductase inhibitors

Sarges,Schnur,Belletire,Peterson

, p. 230 - 243 (2007/10/02)

Sorbitol formation from glucose, catalyzed by the enzyme aldose reductase, is believed to play a role in the development of certain chronic complications of diabetes mellitus. Spiro hydantoin derived from five- and six-membered ketones fused to an aromatic ring or ring system inhibit aldose reductase isolated from calf lens. In vivo these compounds are potent inhibitors of sorbitol formation in sciatic nerves of streptozotocinized rats. Optimum in vivo activity is reached in spiro hydantoins derived from 6-halogenated 2,3-dihydro-4H-1-benzopyran-4-ones (4-chromanones). In 2,4-dihydro-6-fluorospirol[4H-1-benzopyran-4,4'-imidazolidine]-2',5'- ione, the activity resides exclusively in the 4S isomer, compound 115 (CP-45,634, USAN: sorbinil). This compound is currently being used to test, in humans, the value of aldose reductase inhibitors in the therapy of diabetic complications.

Thienohydantoin derivatives

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, (2008/06/13)

Novel spiro-thienohydantoin derivatives useful as aldose reductase inhibitors and as therapeutic agents for the treatment of chronic diabetic complications are disclosed. Preferred compounds include 6,7-dihydro-spiro-[benzo(b)thiophene-4(5H),4'-imidazolidine]-2',5'-dione, 2-chloro-spiro-[cyclopenta(b) thiophene-4,4'-imidazolidine]-2',5'-dione, spiro-[cyclopenta(c)thiophene-4,4'-imidazolidine]-2',5'-dione, 1-chloro-spiro[cyclopenta(c)thiophene-4,4'-imidazolidine]-2',5'-dione and 1,3-dichloro-spiro[cyclopenta(c)thiophene-4,4'-imidazolidine]-2',5'-dione.

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