Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-

Base Information

Chemical Name:Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-
CAS No.:84993-78-2
Molecular Formula:C₉H₁₄ClN₃O₆
Molecular Weight:295.68
Hs Code.:
DSSTox Substance ID:DTXSID00234040
Nikkaji Number:J153.522F
Wikidata:Q76156927

Synonyms:ACO Ser CNU;ICIG 1773;Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-;84993-78-2;BRN 5582070;L-N-((2-Chloroethyl)nitrosocarbamoyl)serine methyl ester acetate (ester);Ester methylique de la O-(acetate)-N-((chloro-2-ethyl)nitrosocarbamoyl)-L-serine;C9H14ClN3O6;ICIG-1773;DTXSID00234040;AKOS040750109;methyl (2S)-3-acetyloxy-2-[[2-chloroethyl(nitroso)carbamoyl]amino]propanoate;LS-144985

Suppliers and Price of Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.42g/cm³
XLogP3:0.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:8
Exact Mass:295.0571129
Heavy Atom Count:19
Complexity:351

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCC(C(=O)OC)NC(=O)N(CCCl)N=O
Isomeric SMILES:CC(=O)OC[C@@H](C(=O)OC)NC(=O)N(CCCl)N=O

Technology Process of Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L-

There total 2 articles about Serine, N-((2-chloroethyl)nitrosocarbamoyl)-, methyl ester, acetate (ester), L- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 84993-73-7
Ester methylique de la O-(acetate)-N-<(chloro-2-ethyl)carbamoyl>-L-serine

: 84993-78-2
Ester methylique de la O-(acetate)-N-<(chloro-2-ethyl)nitrosocarbamoyl>-L-serine

Guidance literature:: With sodium nitrite; In formic acid; at 0 ℃;

Reference yield:

: 84993-71-5
Ester methylique de la N-<(chloro-2-ethyl)carbamoyl>-L-serine

: 84993-78-2
Ester methylique de la O-(acetate)-N-<(chloro-2-ethyl)nitrosocarbamoyl>-L-serine

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / pyridine / 0 °C

2: 96 percent / sodium nitrite / formic acid / 0 °C

With pyridine; sodium nitrite; In formic acid;