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142035-00-5

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142035-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142035-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,3 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142035-00:
(8*1)+(7*4)+(6*2)+(5*0)+(4*3)+(3*5)+(2*0)+(1*0)=75
75 % 10 = 5
So 142035-00-5 is a valid CAS Registry Number.

142035-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminocyclohex-3-ene-1-carboxylic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names CIS-2-AMINO-CYCLOHEX-3-ENECARBOXYLIC ACID 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:142035-00-5 SDS

142035-00-5Downstream Products

142035-00-5Relevant articles and documents

Stereo- and regiocontrolled syntheses of exomethylenic cyclohexane β-amino acid derivatives

Kiss, Loránd,Forró, Eniko,Orsy, Gy?rgy,ábrahámi, Renáta,Fül?p, Ferenc

, p. 21094 - 21101 (2016/01/25)

Cyclohexane analogues of the antifungal icofungipen [(1R,2S)-2-amino-4-methylenecy clopentanecarboxylic acid] were selectively synthesized from unsaturated bicyclic β-lactams by transformation of the ring olefinic bond through three different regio- and s

Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams

Forro, Eniko,Fueloep, Ferenc

, p. 2875 - 2880 (2007/10/03)

Enantiopure β-amino acids 1a-4a and β-lactams 1b-4b were prepared simultaneously through the lipolase-catalysed enantioselective ring opening of unsaturated racemic β-lactams (±)-1-(±)-4. High enantioselectivities (E>200) were observed when the reactions

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