Cas 42786-59-4,4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE

42786-59-4

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Basic information

Product Name: 4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE
Synonyms: 4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE;TIMTEC-BB SBB010419;4-Chloro-6-hydrazino-pyrimidin-5-ylamine ,97%;4-chloro-6-hydrazinylpyrimidin-5-amine
CAS NO:42786-59-4
Molecular Formula: C₄H₆ClN₅
Molecular Weight: 159.58
EINECS: 205-525-8
Product Categories: N/A
Mol File: 42786-59-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 342.7ºC at 760 mmHg
Flash Point: 161.1ºC
Appearance: /
Density: 1.649g/cm3
Vapor Pressure: 7.4E-05mmHg at 25°C
Refractive Index: 1.766
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE(CAS DataBase Reference)
NIST Chemistry Reference: 4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE(42786-59-4)
EPA Substance Registry System: 4-CHLORO-6-HYDRAZINO-PYRIMIDIN-5-YLAMINE(42786-59-4)

Safety Data

Hazard Codes: Xi
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: IRRITANT
PackingGroup: N/A
Hazardous Substances Data: 42786-59-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 42786-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,8 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42786-59:
(7*4)+(6*2)+(5*7)+(4*8)+(3*6)+(2*5)+(1*9)=144
144 % 10 = 4
So 42786-59-4 is a valid CAS Registry Number.

InChI:InChI=1/C4H6ClN5/c5-3-2(6)4(10-7)9-1-8-3/h1H,6-7H2,(H,8,9,10)

42786-59-4Upstream product

5413-85-4 5-amino-4,6-dichloropyridimine

42786-59-4Downstream Products

42786-59-4Relevant academic research and scientific papers

INHIBITORS OF CELLULAR METABOLIC PROCESSES

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Page/Page column 167, (2018/03/25)

The invention provides inhibitor compounds of MAT2A that are useful as therapeutic agents for treating malignancies wherein the compounds have the general formula (I) : wherein ring A, ring B, ring C and, R1 are as described herein.

Niementowski-type synthesis of pyrido[3,2-e][1,2,4]triazines: potent aza-analogs of pyrido[2,3-b]pyrazine fungicides

Crowley, Patrick J.,Lamberth, Clemens,Müller, Urs,Wendeborn, Sebastian,Sageot, Olivia-A.,Williams, John,Bartovi?, Alexander

scheme or table, p. 2652 - 2654 (2010/06/16)

Novel trisubstituted pyrido[3,2-e][1,2,4]triazines have been found to possess similar biological activity to the corresponding pyridopyrazine fungicides against important phytopathogens such as Mycosphaerella graminicola (wheat leaf blotch), Magnaporthe g

Triazolopyrimidine cannabinoid receptor 1 antagonists

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Page/Page column 22-23, (2010/11/25)

The present application describes compounds according to both Formulas I and II, pharmaceutical compositions comprising at least one compound according to either Formula I or II and optionally one or more additional therapeutic agents, and methods of treatment using the compounds according to Formulas I and II both alone and in combination with one or more additional therapeutic agents. The compounds have the following general formulas: including all prodrugs, solvates, pharmaceutically acceptable salts and stereoisomers, wherein R1, R2, R3, R4 and R5 are described herein.

FUNGICIDES BASED ON NITROGEN-CONTAINING HETEROCYCLES

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Page 76, (2008/06/13)

Fungicidal compounds having the general formula (1): formula (1) wherein W, Z and one of X and Y are N and the other one of X and Y is CR8; R8 is H, halo, C1-4 alkyl, C1-4 alkoxy, C1-4 alkylthio or ha

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