Detail of "5815-08-7"

CAS Number:
5815-08-7
Name:
Methanediamine,1-(1,1-dimethylethoxy)-N,N,N',N'-tetramethyl-
Superlist Name:
1-tert-Butoxy-N,N,N',N'-tetramethylmethanediamine
Molecular Structure:
Formula:
C9H22 N2 O
Molecular Weight:
174.28
Synonyms:
Methanediamine,1-tert-butoxy-N,N,N',N'-tetramethyl- (7CI,8CI);1-(1,1-Dimethylethoxy)-N,N,N',N'-tetramethylmethanediamine;1-tert-Butoxy-N,N,N',N'-tetramethylmethanediamine;Bis(dimethylamino)-tert-butoxymethane; Bis(dimethylamino)methyl tert-butylether; Bredereck's reagent; C-tert-Butoxy-N,N,N',N'-tetramethylmethanediamine;t-Butoxybis(dimethylamino)methane; tert-Butoxybis(dimethylamino)methane;tert-Butoxymethylenebis(dimethylamine)
EINECS:
227-383-9
Density:
0.844
Flash Point:
41 ºC
Hazard Symbols:
Risk Codes:
R10;R36/37/38
Transport Information:
UN 1993

Display：

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

Verified-Platinum Supplier 4th Year Platinum
Supplier 3875 Integral
3875

Tel:+86-571-88938639

Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

avilable in gm to Kg scale

Supplier:Globe chemie [ India]

Integral
84

Tel:919960000638

Address:Bavdhan

304 Integral
304

Tel:+91 22 22072526

Address:K.K. Chambers, Sir P. T. Road, Fort, Mumbai - 400 001

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

b-Carboline derivatives: b-Carboline derivatives. Biere, Helmut Dipl Chem Dr (Schering A.-G. , Fed. Rep. Ger. 5815-08-7 is just another one chemical used in this study.). Ger. Offen. DE 3240511 A1 3 May 1984, 15 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07D471-04; A61K031-435. APPLICATION: DE 82-3240511 29 Oct 1982. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The title compds. [I, R, R1 = H, halo, org. group; R2, R4 = H, alkyl, alkoxyalkyl; R3 = Ph, cyano, alkoxycarbonyl, (R5O)2P(O), R6SO2, alkyloxadiazolyl; R5 = alkyl; R6 = alkyl, aryl, amino] were prepd. Thus H2NCH2CO2Et was treated with Me2NCH(OEt)2 and Me3COK to give 54% Me2NCH:C(CO2Et)N:CHNMe2. This was refluxed in HOAc with 1H-indole to give 60% I (R = R1 = R2 = R4 = H, R3 = CO2Et). .

Indole derivatives and their use for further processing to tryptophans and b-carbolines: Indole derivatives and their use for further processing to tryptophans and b-carbolines.Some chemicals with cas registry numbers like 5815-08-7 are also used. Biere, Helmut (Schering A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3240513 A1 3 May 1984, 16 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07D209-12; C07D209-14; C07D209-22; C07D401-12; C07D401-14; C07D403-12; C07D403-14; C07D413-12; C07D413-14; C07D471-04. APPLICATION: DE 82-3240513 29 Oct 1982. DOCUMENT TYPE: Patent CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) Section cross-reference(s): 28 The title indoles I (R - R2 = H, org. group; R3, R5 = H, alkyl, alkoxyalkyl; R4 = Ph, cyano, alkoxycarbonyl, dialkoxyphosphinyl, arylsulfonyl, alkylsulfonyl, dialkylsulfamoyl, oxadiazolyl; R6, R7 = alkyl; NR6R7 = heterocyclyl) were prepd. Thus, Me2NCH(OEt)2 was condensed with H2NCH2CO2Et to give 54% Me2NCH:C(CO2Et)N:CHNMe2. This was stirred 48 h at room temp. in F3CCO2H with 1H-indole to give 35% I (R = R1 = R2 = R3 = R5 = H, R4 = CO2Et, R6 = R7 = Me). I are intermediates for prepn. of b-carbolines and tryptophans. .