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10300-69-3

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10300-69-3 Usage

Uses

Chloroacetamidine hydrochloride is used as a general pharmacophore in delineating characteristics of the amidinotransferase superfamily.

Check Digit Verification of cas no

The CAS Registry Mumber 10300-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,0 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10300-69:
(7*1)+(6*0)+(5*3)+(4*0)+(3*0)+(2*6)+(1*9)=43
43 % 10 = 3
So 10300-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H5ClN2.ClH/c3-1-2(4)5;/h1H2,(H3,4,5);1H

10300-69-3 Well-known Company Product Price

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  • Alfa Aesar

  • (A14835)  2-Chloroacetamidine hydrochloride, 96%   

  • 10300-69-3

  • 1g

  • 255.0CNY

  • Detail
  • Alfa Aesar

  • (A14835)  2-Chloroacetamidine hydrochloride, 96%   

  • 10300-69-3

  • 5g

  • 932.0CNY

  • Detail
  • Alfa Aesar

  • (A14835)  2-Chloroacetamidine hydrochloride, 96%   

  • 10300-69-3

  • 25g

  • 3954.0CNY

  • Detail
  • Aldrich

  • (591475)  Chloroacetamidinehydrochloride  97%

  • 10300-69-3

  • 591475-5G

  • 1,173.51CNY

  • Detail

10300-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name CHLOROACETAMIDINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 2-CHLORORACETAMIDINE 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:10300-69-3 SDS

10300-69-3Relevant articles and documents

IMIDAZOTRIAZINONE COMPOUNDS

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Paragraph 0699; 0700, (2013/10/08)

The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.

Substituted 5-amino-1,2,4-thiadiazoles with pharmaceutical activity

-

, (2008/06/13)

Pharmaceutical compounds of the following formula are described: in which R1 is hydrogen, C1 4 alkyl, C1 4 alkoxy-C1 4 alkyl, hydroxy-C1 4 alkyl, optionally substituted phenyl, optionally substituted phenyl-C1 4 alkyl or a heterocycle selected from: where R3 is hydrogen, C1 4 alkyl, C1 4 alkoxy, nitro, halo, cyano, trifluoromethyl, carboxyl or -CONH2, and R4 is C1 4 alkyl; and R2 is hydrogen, C1 4 alkyl, phenyl or thienyl substituted with a carboxyl or C1 4 alkoxy-carbonyl group, an acyl group of the formula R5CO- where R5 is hydrogen, C1 4 alkyl, C1 4 alkoxy-C1 4 alkyl, halo C1 4 alkyl, C1 4 alkoxy, halo-C1 4 alkoxy, phenyl, phenyl-C1 4 alkyl, -NHC1 4 alkyl, -NH phenyl or where R6 is C1 4 alkyl, or a group of the formula -CH=C(COC1 4 alkoxy)2; or a salt thereof.

Inhibitors of Pyrimidine Biosynthesis. Part 2. The Synthesis of Amidine Phosphonates as Potential Inhibitors of Carbamoyl Phosphate Synthase

Wharton, Clifford J.,Wrigglesworth, Roger

, p. 433 - 436 (2007/10/02)

The synthesis of a series of amidine phosphonates (8) and (9) via a thioimidate intermediate is described.

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