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15719-64-9

15719-64-9

Identification

Synonyms:

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Relevant articles and documentsAll total 2 Articles be found

Fichter,Humpert

, p. 697 ()

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Kharasch,Dannley

, p. 406,410 (1945)

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McDowell,Sharples

, p. 258,260,268 (1958)

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Severson,Brice

, p. 2313,2316 (1958)

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Dunn,Kutschke

, p. 421 (1958)

Strachan,Noyes

, p. 3258 (1954)

Holroyd,Noyes

, p. 4831 (1956)

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Kandel,Taylor

, p. 1250 (1951)

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Szwarc

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Jaeger,Berger

, p. 79 (1922)

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Hoshino et al.

, p. 392,393 (1952)

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Zellner,Lister

, p. 1938,1942,1943 (1956)

Hookway,Selton

, p. 493 (1958)

Levesley,Waters

, p. 217,219 (1955)

Head,Hughes

, p. 2046,2049, 2052 (1952)

Traube,Burmeister,Blaser

, p. 442 (1927)

Thomas,O'Shaughnessy

, p. 455,463 (1953)

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Koller,Pfeiffer

, p. 241,247 (1933)

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Updegraff,Cassidy

, p. 407 (1949)

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Pfau,Plattner

, p. 768,789 (1940)

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Kossel

, (1882)

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Griess

, p. 859 (1875)

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Milas,McAlevy

, p. 1219 (1934)

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Lyford

, p. 1227 (1907)

Allmand,Reeve

, p. 2834,2837, 2843, 2851 (1926)

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Chanmugan,Burton

, p. 509,513,514 (1956)

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Boschan

, p. 3341,3344 (1959)

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Strause,Dyer

, p. 136 (1956)

Hine,Duffey

, p. 1131,1136 (1959)

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Boyer,Morgan

, p. 3012,3015 (1958)

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Fichter,Schnider

, p. 1428,1430, 1433 (1930)

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Adkins,Lazier

, p. 2292,2294 (1924)

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Kondo et al.

, p. 749 (1956)

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Henne,Nager

, p. 650 (1952)

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Rohr,Noyes

, p. 843 (1955)

Guenther,Walters

, p. 1310 (1959)

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Linnell,Noyes

, p. 3863 (1950)

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Prescott et al.

, p. 145 (1954)

Gustus,Lewis

, p. 1512,1516 (1927)

Schubert,Pease

, p. 2044,2047 (1956)

Srinivasan,Noyes

, p. 5591,5592 (1960)

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Hesse

, (1903)

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Porter

, p. 1878 (1957)

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Porter,Cady

, p. 5625 (1957)

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Engfeldt

, p. 38 Anm. (1922)

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Levy,Szwarc

, p. 5981 (1954)

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Burwasser,Taylor

, p. 2295 (1955)

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Wilson,Lippincott

, p. 4290 (1956)

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Fischer,E.,Frank

, p. 2610 (1897)

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Ulpiani,Cingolani

, p. 389 (1904)

Kinetics of the degradation of isoamyl nitrite in ampuls. I. Nature of reaction products and influence of temperature, oxygen, alcohol, water, and acid on the overall rate.

YUNKER,SZULCZEWSKI,HIGUCHI

, p. 613 - 620 (2007/12/05)

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A note on the action of N-bromosuccinimide on aliphatic dicarboxylic acids.

BARAKAT

, p. 582 - 583 (2007/11/09)

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Process route upstream and downstream products

Process route

2-cyano-pent-3-enoic acid

2-cyano-pent-3-enoic acid

2-pentenenitrile
13284-42-9

2-pentenenitrile

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
at 100 ℃;
(4-nitro-phenoxy)-malonic acid
2272-12-0

(4-nitro-phenoxy)-malonic acid

4-nitrophenoxyacetic acid
1798-11-4

4-nitrophenoxyacetic acid

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
at 182 ℃;
benzoyl-(4-methoxy-benzoyl)-peroxide
2900-82-5

benzoyl-(4-methoxy-benzoyl)-peroxide

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

benzoic acid
65-85-0,8013-63-6

benzoic acid

Conditions
Conditions Yield
N-Bromosuccinimide
128-08-5

N-Bromosuccinimide

water
7732-18-5

water

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
di-[1]naphthyl-imidazolidinetrione

di-[1]naphthyl-imidazolidinetrione

1-amino-naphthalene
134-32-7

1-amino-naphthalene

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
2,3,4,5-tetrabromo-tetrahydro-furan-2-carboxylic acid
89284-17-3

2,3,4,5-tetrabromo-tetrahydro-furan-2-carboxylic acid

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

2,2-Dibromo-succinic acid
101349-74-0

2,2-Dibromo-succinic acid

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
water
7732-18-5

water

2,3-oxiranedicarboxylic acid
3272-11-5,51274-37-4

2,3-oxiranedicarboxylic acid

DL-tartaric acid
133-37-9,138508-61-9

DL-tartaric acid

tartaric acid
87-69-4,138508-61-9

tartaric acid

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

Conditions
Conditions Yield
3-bromo-3-methyl-furan-2,4-dione

3-bromo-3-methyl-furan-2,4-dione

water
7732-18-5

water

3-methyl-furan-2,4-dione
1192-51-4,69841-77-6

3-methyl-furan-2,4-dione

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

dimethylglyoxal
431-03-8

dimethylglyoxal

Conditions
Conditions Yield
at 100 ℃;
4-hydroxy-2-keto-4-methylglutaric lactone
512-76-5

4-hydroxy-2-keto-4-methylglutaric lactone

water
7732-18-5

water

bromine
7726-95-6

bromine

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

1-bromoacetone
598-31-2

1-bromoacetone

Conditions
Conditions Yield
3-bromo-2-methyl-4,5-dioxo-tetrahydro-furan-2-carboxylic acid

3-bromo-2-methyl-4,5-dioxo-tetrahydro-furan-2-carboxylic acid

water
7732-18-5

water

bromine
7726-95-6

bromine

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

methylammonium carbonate
15719-64-9,15719-76-3,97762-63-5

methylammonium carbonate

1-bromoacetone
598-31-2

1-bromoacetone

Conditions
Conditions Yield

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