Cas 909702-86-9,3-diMethylbenzyl)cyclopropanaMine hydrochloride

909702-86-9

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Basic information

Product Name: 3-diMethylbenzyl)cyclopropanaMine hydrochloride
Synonyms: 3-diMethylbenzyl)cyclopropanaMine hydrochloride;BenzeneMethanaMine, N-cyclopropyl-2,3-diMethyl-, hydrochloride;N-Cyclopropyl-2,3-dimethylbenzylamine hydrochloride, 3-[(Cyclopropylamino)methyl]-o-xylene hydrochloride
CAS NO:909702-86-9
Molecular Formula: C₁₂H₁₇N*ClH
Molecular Weight: 211.73102
EINECS: N/A
Product Categories: N/A
Mol File: 909702-86-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: Sealed in dry,Room Temperature
Solubility: N/A
CAS DataBase Reference: 3-diMethylbenzyl)cyclopropanaMine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 3-diMethylbenzyl)cyclopropanaMine hydrochloride(909702-86-9)
EPA Substance Registry System: 3-diMethylbenzyl)cyclopropanaMine hydrochloride(909702-86-9)

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: 909702-86-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909702-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,7,0 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 909702-86:
(8*9)+(7*0)+(6*9)+(5*7)+(4*0)+(3*2)+(2*8)+(1*6)=189
189 % 10 = 9
So 909702-86-9 is a valid CAS Registry Number.

909702-86-9Upstream product

625437-38-9 cyclopropyl-(2,3-dimethyl-benzyl)-amine

909702-86-9Downstream Products

1041438-90-7 cyclopropyl-2,3-dimethylbenzylacetamide

909702-86-9Relevant academic research and scientific papers

A PROCESS FOR PREPARING DIAZABICYCLO[3.3.1] NONANE COMPOUNDS

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Page/Page column 11; 15-16, (2008/12/07)

The invention is a process for preparing a diazabicyclo compound of formula (I) process for preparing a diazabicyclo compound of formula (I):where X is selected from the group consisting of hydrogen, C1-C6 alkoxycarbonyl, and carbobenzyloxy; R6 is selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and benzyl; and R9, R 10, and R11 are independently selected from the group consisting of hydrogen, halogen, and C1-C6 alkyl. wherein the process involves cyclizing I-I, formula (II).

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