Basic information

Product Name: Acetamide, N-(cyclohexylmethyl)-2-diazo-N-(1,1-dimethylethyl)-
Synonyms:
CAS NO:650599-20-5
Molecular Formula: C13H23N3O
Molecular Weight: 237.345
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetamide, N-(cyclohexylmethyl)-2-diazo-N-(1,1-dimethylethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, N-(cyclohexylmethyl)-2-diazo-N-(1,1-dimethylethyl)-(650599-20-5)
EPA Substance Registry System: Acetamide, N-(cyclohexylmethyl)-2-diazo-N-(1,1-dimethylethyl)-(650599-20-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 650599-20-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 650599-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,5,9 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 650599-20:
(8*6)+(7*5)+(6*0)+(5*5)+(4*9)+(3*9)+(2*2)+(1*0)=175
175 % 10 = 5
So 650599-20-5 is a valid CAS Registry Number.

650599-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-[tert-butyl(cyclohexylmethyl)amino]-2-diazonioethenolate

1.2 Other means of identification

Product number	-
Other names	Acetamide,N-(cyclohexylmethyl)-2-diazo-N-(1,1-dimethylethyl)

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).

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650599-20-5Relevant academic research and scientific papers

The synthesis of baclofen and GABOB via Rh(II) catalyzed intramolecular C-H insertion of α-diazoacetamides

Chen, Zhenliang,Chen, Zhiyong,Jiang, Yaozhong,Hu, Wenhao

, p. 1579 - 1586 (2005)

The synthesis of baclofen and GABOB is reported via hydrolysis of the corresponding N-tert-butyl γ-lactams, which were obtained from Rh(II) catalyzed intramolecular C-H insertion of α-diazoacetamides.

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