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78946-84-6

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78946-84-6 Usage

General Description

"(11R*,15R*)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane" is a chemical compound with a complex structure consisting of a 13-membered ring containing four oxygen atoms and one nitrogen atom. It has two chiral centers at positions 11 and 15, which gives rise to four possible stereoisomers. (11R*,15R*)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane belongs to the class of heterocycles, containing both oxygen and nitrogen atoms in the ring. It is a cyclic ether with a nitrogen atom incorporated into the ring structure. (11R*,15R*)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane may have potential applications in medicinal chemistry, material science, or as a reagent in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 78946-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78946-84:
(7*7)+(6*8)+(5*9)+(4*4)+(3*6)+(2*8)+(1*4)=196
196 % 10 = 6
So 78946-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H25NO4/c1-11-9-13-10-12(2)17-8-6-15-4-3-14-5-7-16-11/h11-13H,3-10H2,1-2H3

78946-84-6SDS

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 (11R,15R)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane

1.2 Other means of identification

Product number -
Other names EINECS 279-012-5

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78946-84-6 SDS

78946-84-6Downstream Products

78946-84-6Relevant articles and documents

Synthesis of Monoaza Crown Ethers from N,N-Diamines and Oligoethylene Glycol Di(p-toluenesulfonates) or Corresponding Dichlorides

Maeda, Hirokazu,Furuyoshi, Shigeo,Nakatsuji, Yohji,Okahara, Mitsuo

, p. 212 - 218 (2007/10/02)

Monoaza crown ethers were prepared in satisfactory yields by the one-step reaction between diethanolamine or N,N-diamines and oligoethylene glycol di(p-toluenesulfonates) or corresponding dichlorides in t-butyl alcohol/dioxane in the presence of sodium or potassium t-butoxide.The reaction conditions in the preparation of monoaza 15- and 18-crown ethers were studied.Various monoaza crown ethers having substituents were also prepared and their properties were investigated.

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