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59855-11-7

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59855-11-7 Usage

Chemical Properties

white fine powder

Purification Methods

Recrystallise the salt from EtOH. The free base [2835-68-9] M 136.2, has m 182.9o and crystallises with 0.25H2O (m 178-179o). [Rupe & Vogler Helv Chim Acta 8 835 1925, Beilstein 14 H 425, 14 III 1061.]

Check Digit Verification of cas no

The CAS Registry Mumber 59855-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,5 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59855-11:
(7*5)+(6*9)+(5*8)+(4*5)+(3*5)+(2*1)+(1*1)=167
167 % 10 = 7
So 59855-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O.ClH/c9-7(10)5-1-3-6(4-2-5)8(11)12;/h1-4H,(H3,9,10)(H2,11,12);1H

59855-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amidinobenzamide hydrochloride

1.2 Other means of identification

Product number -
Other names P-AMIDINOBENZAMIDE HYDROCHLORIDE

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:59855-11-7 SDS

59855-11-7Relevant articles and documents

Therapeutic quinazoline derivatives

-

, (2008/06/13)

A compound of formula (I) or a salt, ester, amide or prodrug thereof; where X is O, or S, S(O), S(O)2 or NR6 where R6 is hydrogen of C1-6alkyl; R5 is an optionally substituted 6-membered aromatic ring containing at least one nitrogen atom, and R1, R2, R3, R4 are independently selected from halogeno, cyano, nitro, C1-3alkylsulphanyl, —N(OH)R7— (wherein R7 is hydrogen, or C1-3alkyl), or R9X1— (wherein X1 represents a direct bond, —O—, —CH2—, —OC(O), —C(O)—, —S—, —SO—, —SO2—, —NR10C(O)—, —C(O)NR11—, —SO2NR12—, —NR13SO2— or NR14— (wherein R10, R11, R12, R13 and R14 each independently represents hydrogen, C1-3alkyl or C1-3alkoxyC2-3alkyl), and R9 is hydrogen, optionally substituted hydrocarbyl, optionally substituted heterocyclyl or optionally substituted alkoxy; provided that at least one of R2 or R3 is other than hydrogen. These compounds inhibit aurora 2 kinase and are useful in the preparation of medicaments for the treatment of proliferative disease such as cancer.

Heterobiarly derivatives and pharmaceutical compositions thereof

-

, (2008/06/13)

Heterobiaryl derivatives of the formula wherein R1, X1 to X3 and Y1 to Y4 are as defined herein, the tautomers, stereoisomers and mixtures thereof, and the salts, particularly the physiologica

Pyrimidine derivatives

-

, (2008/06/13)

Optically active pyrimidines of the formula STR1 wherein Z is --(CH2)n -- or --(CH2)n --O-- wherein n is an integer of 1 to 4 and each of the symbols X is a nitrogen atom and each of the symbols Y is --CH-- or e

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