Cas 1609949-22-5,6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate

1609949-22-5

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Basic information

Product Name: 6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate
Synonyms: 6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate
CAS NO:1609949-22-5
Molecular Formula:
Molecular Weight: 434.557
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: 6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate(CAS DataBase Reference)
NIST Chemistry Reference: 6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate(1609949-22-5)
EPA Substance Registry System: 6-(((benzyloxy)carbonyl)amino)-6-methyl-1-phenylheptan-3-yl sulfamate(1609949-22-5)

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: 1609949-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609949-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,9,4 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1609949-22:
(9*1)+(8*6)+(7*0)+(6*9)+(5*9)+(4*4)+(3*9)+(2*2)+(1*2)=205
205 % 10 = 5
So 1609949-22-5 is a valid CAS Registry Number.

1609949-22-5Upstream product

1609948-98-2 C₂₂H₂₉NO₃

1609949-22-5Downstream Products

1609949-22-5Relevant academic research and scientific papers

Synthesis of heterocycles based on rhodium-catalyzed C-H amination

Takahashi, Keisuke,Yamaguchi, Daisuke,Ishihara, Jun,Hatakeyama, Susumi

, p. 133 - 137 (2014)

A new stereoselective approach to substituted pyrrolidines and piperidines is described that involves Du Bois' C-H -amination reaction, Boc-activation of a cyclic sulfamate group, and base-promoted intramolecular cyclization. This methodology can be utilized for the synthesis of tetrahydrofuran and tetrahydrothiophene derivatives. Georg Thieme Verlag Stuttgart · New York.

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