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N,N-DIBOC-4-AMINO-6-CHLOROPYRIMIDINE is a chemical compound that serves as a key intermediate in organic synthesis and pharmaceutical research. As a derivative of pyrimidine, it is integral to the structure of nucleic acids like DNA and RNA. Its chloropyrimidine moiety endows it with unique properties, making it a valuable building block in the development of pharmaceuticals and agrochemicals. N,N-DIBOC-4-AMINO-6-CHLOROPYRIMIDINE is also utilized as a reagent in organic chemistry for the synthesis of new compounds with potential applications in pharmacology and agriculture.

354112-08-6

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  • Imidodicarbonicacid,2-(6-chloro-4-pyrimidinyl)-,1,3-bis(1,1-dimethylethyl) ester

    Cas No: 354112-08-6

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354112-08-6 Usage

Uses

Used in Pharmaceutical Research and Development:
N,N-DIBOC-4-AMINO-6-CHLOROPYRIMIDINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the creation of biologically active molecules. Its presence in the molecular structure of drugs aids in the development of new therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, N,N-DIBOC-4-AMINO-6-CHLOROPYRIMIDINE is used as a building block for the synthesis of agrochemicals, contributing to the development of new compounds that can enhance crop protection and yield.
Used in Organic Chemistry as a Reagent:
N,N-DIBOC-4-AMINO-6-CHLOROPYRIMIDINE is utilized as a reagent in organic chemistry reactions, facilitating the creation of novel compounds with potential pharmacological and agricultural applications. Its versatility in chemical reactions makes it a valuable tool for researchers in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 354112-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,1,1 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 354112-08:
(8*3)+(7*5)+(6*4)+(5*1)+(4*1)+(3*2)+(2*0)+(1*8)=106
106 % 10 = 6
So 354112-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H20ClN3O4/c1-13(2,3)21-11(19)18(12(20)22-14(4,5)6)10-7-9(15)16-8-17-10/h7-8H,1-6H3

354112-08-6SDS

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 tert-butyl N-(6-chloropyrimidin-4-yl)-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate

1.2 Other means of identification

Product number -
Other names W5704

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:354112-08-6 SDS

354112-08-6Downstream Products

354112-08-6Relevant articles and documents

Structure-based Design of Pyridone-Aminal eFT508 Targeting Dysregulated Translation by Selective Mitogen-activated Protein Kinase Interacting Kinases 1 and 2 (MNK1/2) Inhibition

Reich, Siegfried H.,Sprengeler, Paul A.,Chiang, Gary G.,Appleman, James R.,Chen, Joan,Clarine, Jeff,Eam, Boreth,Ernst, Justin T.,Han, Qing,Goel, Vikas K.,Han, Edward Z. R.,Huang, Vera,Hung, Ivy N. J.,Jemison, Adrianna,Jessen, Katti A.,Molter, Jolene,Murphy, Douglas,Neal, Melissa,Parker, Gregory S.,Shaghafi, Michael,Sperry, Samuel,Staunton, Jocelyn,Stumpf, Craig R.,Thompson, Peggy A.,Tran, Chinh,Webber, Stephen E.,Wegerski, Christopher J.,Zheng, Hong,Webster, Kevin R.

, p. 3516 - 3540 (2018/05/01)

Dysregulated translation of mRNA plays a major role in tumorigenesis. Mitogen-activated protein kinase interacting kinases (MNK)1/2 are key regulators of mRNA translation integrating signals from oncogenic and immune signaling pathways through phosphoryla

Isoindoline, azaisoindoline, dihydroindenone and dihydroazaindenone inhibitors of Mnk1 and Mnk2

-

Page/Page column 44, (2018/11/21)

The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula I, or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof. For Formula I compounds A1, A2

ANTI-ANGIOGENESIS COMPOUND, INTERMEDIATE AND USE THEREOF

-

Paragraph 0076; 0077, (2016/04/10)

Disclosed are an anti-abnormal proliferation of angiogenesis compound represented by formula I, use and intermediate thereof. The compound has good effect against abnormal proliferation of angiogenesis, and the activity of the compound is produced by inhibiting VEGFR2. The compound can be used for treating diseases, such as wet macular degeneration, inflammation, malignant tumor and the like, caused by abnormity of angiogenesis and protein kinases such as VEGFR2, FGFR2 and the like.

ANTI-ANGIOGENESIS COMPOUND, INTERMEDIATE AND USE THEREOF

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Paragraph 0093; 0096-0098, (2016/11/02)

Disclosed are an anti-abnormal proliferation of angiogenesis compound represented by formula I, use and intermediate thereof. The compound has good effect against abnormal proliferation of angiogenesis, and the activity of the compound is produced by inhibiting VEGFR2. The compound can be used for treating diseases, such as wet macular degeneration, inflammation, malignant tumor and the like, caused by abnormity of angiogenesis and protein kinases such as VEGFR2, FGFR2 and the like.

Α 7 as intranuclear hydroxynicotinic acetylcholine receptor quinuclidines compd.

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Paragraph 0653; 0654, (2018/10/03)

PROBLEM TO BE SOLVED: To provide ligands for the nicotinic α-7 receptor used for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.SOLUTION: The disclosure provides compounds of the specified formula I, including their salts, and compositions and methods using the compounds.

HETEROCYCLIC COMPOUND

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Paragraph 0673, (2015/01/18)

The present invention provides an agent for the prophylaxis or treatment of autoimmune diseases (e.g., psoriasis, rheumatoid arthritis, inflammatory bowel disease, Sjogren's syndrome, Behcet's disease, multiple sclerosis, systemic lupus erythematosus etc.) and the like, which has a superior Tyk2 inhibitory action. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the specification, or a salt thereof.

PYRAZOLOPYRIDINES AND PYRAZOLOPYRIDINES AND THEIR USE AS TYK2 INHIBITORS

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Page/Page column 174, (2012/06/01)

The invention provides compounds of Formula (I), stereoisomers or pharmaceutically acceptable salts thereof, wherein A, X, R1, R2, R4 and R5 are defined herein, a pharmaceutical composition that includes a compound of Formula (I) and a pharmaceutically acceptable carrier, adjuvant or vehicle, and methods of using the compound or composition in therapy, as TYK2 Kinase inhibitors.

Two-level self-organisation of arrays of [2x2] grid-type tetranuclear metal complexes by hydrogen bonding

Breuning, Esther,Ziener, Ulrich,Lehn, Jean-Marie,Wegelius, Elina,Rissanen, Kari

, p. 1515 - 1521 (2007/10/03)

Here we report on the synthesis and characterisation of four new complexes of the [2x2] M4II grid-type (M = Co, Fe, Zn) with oligopyridine-derived ligands. The presence of aminopyrazine and aminopyrimidine moieties at the edge of the ligands potentially enables the formation of infinite hydrogen-bonded multi-grid networks. The ligands were synthesised by subsequent stannylations and Stille-type coupling reactions. The complexes were obtained by self-assembly of the ligand with the metal salt. The single-crystal X-ray structure was determined for the Co complex 7 containing aminopyrimidine as the hydrogen-bonding moiety [P1; a = 15.4976(4), b = 18.2114(6), c = 31.9538(10) A, α = 86.9809(13), β = 83.4137(18), γ = 67.2828(16)°]. The crystal structure reveals hydrogen bonding in one direction, thus forming infinite chains of grids, whereas in the second direction of a layer, only weak attractive interactions are found. Anions and solvent molecules are situated between the layers, thus inhibiting any direct interaction between them. Cocrystallisation of the complementary complexes should enable the recognition-controlled alternating arrangement of grids incorporating different metal ions in a chessboard-like manner. Wiley-VCH Verlag GmbH, 2001.

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