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145028-12-2

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145028-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145028-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,2 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145028-12:
(8*1)+(7*4)+(6*5)+(5*0)+(4*2)+(3*8)+(2*1)+(1*2)=102
102 % 10 = 2
So 145028-12-2 is a valid CAS Registry Number.

145028-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N'-(α-methylamino-α-methoxy-methylene)- hydrazine-N-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl N'-(α-methylamino-α-methoxy-methylene)-hydrazine-N-carboxylate

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:145028-12-2 SDS

145028-12-2Upstream product

145028-12-2Downstream Products

145028-12-2Relevant articles and documents

Process for the preparation of alkoxytriazolinones

-

, (2008/06/13)

Alkoxytriazolinones of the general formula (I), STR1 in which R1 and R2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, (which can be used as intermediates for the preparation of herbicidal active compounds) are obtained in very good yields and in high purity by reacting iminothiocarbonic diester (II) with carbazinic esters (III) STR2 in which R3 and R4 in each case represent, for example, alkyl or aryl, at -20° C. to +50° C. (1st step) and subjecting the semicarbazide derivatives (IV) formed in this process with elimination of R3 -SH STR3 to a cyclizing condensation reaction and if appropriate in the presence of a base at 20° C. to 100° C. with elimination of R4 --OH, if appropriate after intermediate isolation (2nd step).

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