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1-benzyloxy-3-amino-4,6-dinitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1313038-08-2

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1313038-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313038-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,0,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1313038-08:
(9*1)+(8*3)+(7*1)+(6*3)+(5*0)+(4*3)+(3*8)+(2*0)+(1*8)=102
102 % 10 = 2
So 1313038-08-2 is a valid CAS Registry Number.

1313038-08-2Relevant academic research and scientific papers

2,4,5-TRIAMINOPHENOLS AND RELATED COMPOUNDS

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, (2013/03/26)

New triaminophenol compositions and related compounds are disclosed, as are processes for their preparation and for the preparation of novel salts and diacid complexes from such compounds. Polymers prepared from these compositions can be made into high strength fiber, film, and tape and are useful in applications such as protective apparel, aircraft, automotive components, personal electronics, and sports equipment.

2,4,5-TRIAMINOPHENOLS AND RELATED COMPOUNDS

-

, (2013/03/26)

New triaminophenol compositions and related compounds are disclosed, as are processes for their preparation and for the preparation of novel salts and diacid complexes from such compounds. Polymers prepared from these compositions can be made into high strength fiber, film, and tape and are useful in applications such as protective apparel, aircraft, automotive components, personal electronics, and sports equipment.

INTEGRATED PROCESSES FOR THE PREPARATION OF POLYBENZIMIDAZOLE PRECURSORS

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Page/Page column 29-30, (2011/08/03)

An integrated process is provided for efficiently preparing 2,4,5-triaminophenol, starting with nitration of 2,6-dihalobenzene; high purity salts thereof; and complexes of 2,4,5-triaminophenol aromatic diacids, which are precursors for making polybenzimid

2,4,5-TRIAMINOPHENOLS AND RELATED COMPOUNDS

-

, (2011/08/03)

New triaminophenol compositions and related compounds are disclosed, as are processes for their preparation and for the preparation of novel salts and diacid complexes from such compounds. Polymers prepared from these compositions can be made into high strength fiber, film, and tape and are useful in applications such as protective apparel, aircraft, automotive components, personal electronics, and sports equipment.

2,4,5-TRIAMINOPHENOLS AND RELATED COMPOUNDS

-

, (2011/08/03)

New triaminophenol compositions and related compounds are disclosed, as are processes for their preparation and for the preparation of novel salts and diacid complexes from such compounds. Polymers prepared from these compositions can be made into high strength fiber, film, and tape and are useful in applications such as protective apparel, aircraft, automotive components, personal electronics, and sports equipment.

2,4,5-TRIAMINOPHENOLS AND RELATED COMPOUNDS

-

, (2011/08/03)

New triaminophenol compositions and related compounds are disclosed, as are processes for their preparation and for the preparation of novel salts and diacid complexes from such compounds. Polymers prepared from these compositions can be made into high strength fiber, film, and tape and are useful in applications such as protective apparel, aircraft, automotive components, personal electronics, and sports equipment.

INTEGRATED PROCESSES FOR THE PREPARATION OF POLYBENZIMIDAZOLE PRECURSORS

-

Page/Page column 27-28, (2011/08/03)

An integrated process is provided for efficiently preparing 2,4,5-triaminophenol, starting with nitration of 2,6-dihalobenzene; high purity salts thereof; and complexes of 2,4,5-triaminophenol aromatic diacids, which are precursors for making polybenzimidazole polymer for high performance fibers. The process design eliminates several costly intermediate drying and recrystallization steps. The handling of solid materials with possible skin sensitizing properties and toxicity is avoided, thereby eliminating human and environmental exposure.

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