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Octahydro-pyrrolo[3,4-b]pyrrole is a heterocyclic organic compound with the molecular formula C8H15N. It is a saturated, nitrogen-containing ring structure derived from pyrrole, which is a five-membered aromatic ring with two carbon atoms and two nitrogen atoms. OCTAHYDRO-PYRROLO[3,4-B]PYRROLE is characterized by its octahydro prefix, indicating the presence of eight hydrogen atoms attached to the carbon atoms in the ring, making it a fully saturated derivative. Octahydro-pyrrolo[3,4-b]pyrrole is of interest in organic chemistry and may have potential applications in the synthesis of more complex molecules and pharmaceuticals due to its unique structure and properties.

931-00-0

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931-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 931-00-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 931-00:
(5*9)+(4*3)+(3*1)+(2*0)+(1*0)=60
60 % 10 = 0
So 931-00-0 is a valid CAS Registry Number.

931-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,3a,4,5,6,6a-octahydropyrrolo[2,3-c]pyrrole

1.2 Other means of identification

Product number -
Other names 2,7-Diaza-bicycl<0.3.3>octan

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:931-00-0 SDS

931-00-0Downstream Products

931-00-0Relevant academic research and scientific papers

Novel heterocyclic antibacterial compounds

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, (2008/06/13)

The invention provides heterocyclic organic compounds that inhibit bacterial DNA polymerase IIIC and type II bacterial topoisomerase. The invention further provides compounds that are useful as intermediates in the synthesis of such heterocyclic organic compounds. Syntheses and uses of such heterocyclic organic molecules are also described.

Preparation of 2,7-diazabicyclo[3.3.0]octanes

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, (2008/06/13)

2,7-Diazabicyclo[3.3.0]octanes, suitable for 7-position substituents or antibacterially active quinolone carboxylic acids, of the formula STR1 in which R1, R3, R4, R5, R7 and R8 may be identical or different and in each case denote H, C1 -C5 -alkyl (optionally substituted by halogen, hydroxyl or C1 -C3 -alkoxy), C1 -C3 -alkoxycarbonyl or C6 -C12 -aryl, R4 additionally denotes halogen, R2 and R6 may be identical or different, denote H, C1 -C6 -alkyl, benzyl, C6 -C12 -aryl, C1 -C3 -alkanoyl, benzoyl or C1 -C5 -alkoxycarbonyl, or R2 and R3 together denote a bridge of the structure (CH2)n, n=2-4, CH2 --CHOH--CH2, CH2 --S--CH2 or C(CH3)2 --S--CH2, excluding 2,7-diazabicyclo[3.3.0]octane. Also their preparation by the reaction STR2 Intermediates II are also new.

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