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1578-96-7

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1578-96-7 Usage

General Description

(1-Methyl-1H-indazol-3-yl)methanol is a synthetic compound and belongs to the class of organic compounds known as indazoles, which are aromatic heterocyclic compounds containing a pyrazole ring fused to a benzene ring. It is characterized by a 1H-indazole moiety, where a hydrogen atom at the third position is replaced by a methanol group, and the nitrogen atom at the first position is substituted by a methyl group. While there is not much information available on its properties or uses, it is typically involved in laboratory research and is not naturally occurring. As with all chemicals, it should be handled with appropriate safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 1578-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1578-96:
(6*1)+(5*5)+(4*7)+(3*8)+(2*9)+(1*6)=107
107 % 10 = 7
So 1578-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O/c1-11-9-5-3-2-4-7(9)8(6-12)10-11/h2-5,12H,6H2,1H3

1578-96-7SDS

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-methylindazol-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 1H-Indazole-3-methanol,1-methyl

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:1578-96-7 SDS

1578-96-7Relevant articles and documents

Novel rearrangement of pyrazole N imines with acetic anhydride

Koga,Hirobe,Okamoto

, p. 2267 - 2269 (1976)

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ARYL SUBSTITUTED OLEFINIC COMPOUNDS AS PDE10A INHIBITORS

-

Page/Page column 51, (2011/11/30)

The present invention provides aryl substituted olefinic compounds as Phosphodiesterase 1 0A (PDE 1 0A) inhibitors. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders by inhibiting Phospho

CCK or gastrin modulating benzo ?b!?1,4! diazepines derivatives

-

, (2008/06/13)

Benzo?b!?1,4!diazepine compounds of formula (I), where R1 is selected from C1 C6 alkyl, C3 -C6 cycloalkyl, phenyl, or substituted phenyl; R2 is selected from C3 -C6 alkyl, C3 C6 cycloalkyl, C3 -C6 alkenyl, benzyl, phenylC1 -C3 alkyl of substituted phenyl; or NR1 R2 together form 1,2,3,4-tetrahydroquinoline or benzazepine, mono-, di-, or trisubstituted independently with C1-6 alkyl C1-6 alkoxy or halogen substituents; p is an integer 0 or 1; q is an integer 0 or 1; r is an integer 0 or 1; t is an integer 0 or 1, provided that when r is 0 then t is 0; R3, R5, and R6 are independently hydrogen or C1-6 alkyl; R4 is C1-6 alkyl or C1-6 alkenyl; R7 is selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 cycloalkyl, C1-6 alkenyl, phenyl, substituted phenyl, napthyl, heteroaryl, substituted heteroaryl, bicycloheteroaryl or substituted bicycloheteroaryl; or NR6 R7 together form a saturated 5,6, or 7 membered ring optionally interrupted by 1,2,3 or 4 N, S or O heteroatoms, with the proviso that any two O or S atoms are not bonded to each other, m is an integer selected from the group of 0, 1, 2, 3 or 4; R8 and R9 are selected from a variety of substituents; Z is hydrogen or halogen; novel intermediates, a pharmaceutical composition for treating obesity, gall bladder stasis, disorders of pancreatic secretion, methods for such treatment and processes for preparing compounds of formula (I).

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