Detail of "22483-09-6"

CAS Number:
22483-09-6
Name:
2,2-Dimethoxyethylamine
Molecular Structure:
Formula:
C₄H₁₁NO₂
Molecular Weight:
105.14
Synonyms:
Acetaldehyde,amino-, dimethyl acetal (6CI,8CI);Ethylamine, 2,2-dimethoxy- (8CI);1-Amino-2,2-dimethoxyethane;Aminoacetaldehyde dimethyl acetal;
EINECS:
245-026-5
Density:
0.944 g/cm³
Boiling Point:
133 °C at 760 mmHg
Flash Point:
53.3 °C
Solubility:
miscible with water
Appearance:
clear colorless to pale yellow liquid
Hazard Symbols:
C,F,Xi
Risk Codes:
10-34-36/37/38
Safety:
26-36/37/39-45-16-36 Details
Transport Information:
UN 1993 3/PG 3

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Imidazo[1,2-a]-s-triazine nucleosides: Imidazo[1,2-a]-s-triazine nucleosides. Synthesis and antiviral activity of the N-bridgehead guanine, guanosine, and guanosine monophosphate analogs of imidazo[1,2-a]-s-triazine. Kim, Sun-Hyuk; Bartholomew, David G.; Allen, Lois B.; Robins, Roland K.; Revankar, Ganapathi R.; Dea, Phoebe (Nucleic Acid Res. Inst., ICN Pharm., Inc., Irvine, Calif., USA). J. Med. Chem., 21(9), 883-9 (English) 1978. CODEN: JMCMAR. ISSN: 0022-2623. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Section cross-reference(s): 28, 33 Aminoimidazotriazinone I [67410-64-4] was prepd. by selective amination of cyanuric chloride, followed by the controlled hydrolysis of 2-amino-4,6-dichloro-s-triazine [933-20-0], followed by condensation with H2NCH2CH(OMe)2 [22483-09-6] to giveII [R = CH2CH(OMe)2] [67410-53-1]; hydrolysis of the acetal groups gave II (R = CH:CHOH) [67410-54-2] which was then cyclized. Treatment of I with 1-O-acetyl-2,3,5-tri-O-benzoyl-b-D-ribofuranose and subsequent deblocking gave the nucleoside III (R1 = H) [67410-65-5], which was treated with (MeO)3PO and POCl3 to give the nucleotide III [R1 = P(O)(OH)2] [67410-66-6]. III analogs and imidazo[1,2-a]-s-triazine-2,4-dione [67410-57-5] were similarly prepd. I and III (R1 = H) had moderate antiviral activity and III [R1 = P(O)(OH)2] had slight activity against type 1 herpes, type 13 rhino, and type 3 parainfluenza viruses in culture.Several substances are used for example 67410-64-4 which is its cas registry number.Some commonly used reagents like 67410-64-4 is used in this experiment. ..

(±)-4-Oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline derivatives: (±)-4-Oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline derivatives.Some chemicals with cas registry numbers like 22483-09-6 and 90142-12-4 are also used. Kim, Chung Sup; Lee, Nam Jin; Kim, Jung Hyup (Korea Advanced Institute of Science and Technology, S. Korea). Ger. Offen. DE 3324532 A1 19 Jan 1984, 19 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07D471-04. APPLICATION: DE 83-3324532 7 Jul 1983. PRIORITY: KR 82-3036 8 Jul 1982; KR 83-2418 31 May 1983. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Improved methods for synthesis of title compds. (I; R = H, C1-6 alkyl, acyl; R1, R2 = H, C1-6 alkyl, alkoxy) by cyclization of QNHCOCH2NRCH2CH(OR3)2 or QN[CH2CH(OR3)2]COCH2NHCOR4 [Q = 3,4-R1R2C6H3CH2CH2; R3 = Me, Et, or (R3)2 = CH2; R4 = H, C1-6 alkyl, cycloalkyl, aryl] were developed. Thus, ClCH2CONHCH2CH2C6H3(OMe)2-3,4 was condensed with H2NCH2CH(OMe)2 and then treated with H2SO4 at room temp. to give 96% II. .

Detail of "22483-09-6"

2,2-Dimethoxyethylamine

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CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

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CAS No.22483-09-6 2,2-Dimethoxyethylamine

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CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

CAS No.22483-09-6 2,2-Dimethoxyethylamine

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