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56-39-3

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56-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56-39-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56-39:
(4*5)+(3*6)+(2*3)+(1*9)=53
53 % 10 = 3
So 56-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)/i2+2

56-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoacetic acid

1.2 Other means of identification

Product number -
Other names <1-14C>glycine

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:56-39-3 SDS

56-39-3Upstream product

56-39-3Downstream Products

56-39-3Relevant articles and documents

Preparation method of glycin-1-14C

-

Paragraph 0014; 0033; 0035; 0036; 0038, (2021/10/13)

The invention discloses a preparation method of glycin-1-14C, which comprises the following steps: (1) under the protection of inert gas, enabling anhydrous nitromethane and metal or a metal organic reagent to form a nitromethane salt solution in an anhydrous ether solvent, and then reacting the nitromethane salt solution with CO2 to obtain a crude product of nitroacetic acid-1-C, wherein the CO2 is obtained by acidolysis of barium carbonate C; and (2) under the action of a palladium-carbon catalyst, carrying out reduction reaction on the crude product of the nitroacetic acid-1-C and hydrogen, and after the reaction is finished, carrying out post-treatment to obtain the glycin-1-C. The method has the advantages of short synthesis steps, mild and controllable reaction conditions, no need of high temperature, high pressure and other harsh conditions, no need of use of highly corrosive, highly toxic and other dangerous chemicals, easy trace synthesis, low cost and high C utilization rate, and the finally purified product has the advantages of high purity, good state and small specific activity reduction.

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