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879499-96-4

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879499-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879499-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,4,9 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 879499-96:
(8*8)+(7*7)+(6*9)+(5*4)+(4*9)+(3*9)+(2*9)+(1*6)=274
274 % 10 = 4
So 879499-96-4 is a valid CAS Registry Number.

879499-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethylethyl ((1S)-3-(methylthio)-1-{[(1-oxo-2,3-dihydro-1H-inden-5-yl)amino]carbonyl}propy)carbamate

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:879499-96-4 SDS

879499-96-4Downstream Products

879499-96-4Relevant articles and documents

N-(1-(2,3-DIHYDRO-1H-INDEN-5YL) -2-OXO-3-PYRROLIDINYL) -SULFONAMIDE DERIVATIVES FOR USE AS FACTOR XA INHIBITORS

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Page/Page column 28-29, (2010/10/20)

The invention relates to at least one chemical entity chosen from compounds of formula (I): wherein: R1 represents a group selected from (II): each ring of which optionally contains a further heteroatom N, Z represents an optional substituent halogen, alk represents alkylene or alkenylene, T represents S, O or NH; R2 represents hydrogen, -C1-6alkyl, - C1-3alkyl CONRaRb, - C1-3alkyl CO2 C1-4alkyl, -CO2 C1-4alkyl or - C1-3alkyl CO2H; Ra and Rb independently represent hydrogen, - C1-6alkyl, or together with the N atom to which they are bonded form a 5-, 6- or 7- membered non-aromatic heterocyclic ring optionally containing an additional heteroatom selected from O, N and S, optionally substituted by C1-4alkyl, and optionally the S heteroatom is substituted by O, i.e. represents S(O)n; n represents 0-2; X represents an optional substituent on the indane ring selected from: halogen, - C1-4alkyl, -C2-4alkenyl and -CF3; Y represents a group -(CH2)mNRcRd substituted on the non-aromatic portion of the indane ring; Rc and Rd independently represent hydrogen, - C1-6alkyl, - C1-4alkylOH, or together with the N atom to which they are bonded form a 4-, 5-, 6- or 7- membered non-aromatic heterocyclic ring, the 5-, 6- or 7- membered non-aromatic heterocyclic ring optionally containing an additional heteroatom selected from O, N or S, and the 4-, 5-, 6- or 7- membered non-aromatic heterocyclic ring optionally substituted by C1-4alkyl or halogen; m represents 0-2; and pharmaceutically acceptable derivative(s) thereof. The invention also relates to processes for the preparation of compound(s) of formula (I), pharmaceutical compositions containing compound(s) of formula (I) and to the use of compound(s) of formula (I) in medicine, particularly in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated.

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