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Sigma-Aldrich

Aniline-4-13C

99 atom % 13C

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Synonym(s):
Benzenamine-4-13C
Linear Formula:
13CC5H4NH2
CAS Number:
55147-71-2
Molecular Weight:
93.11
MDL number:
MFCD01075584
PubChem Substance ID:
329758443

isotopic purity

99 atom % 13C

bp

184 °C (lit.)

mp

-6 °C (lit.)

density

1.033 g/mL at 25 °C

mass shift

M+1

storage temp.

2-8°C

SMILES string

Nc1cc[13cH]cc1

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i1+1

InChI key

PAYRUJLWNCNPSJ-OUBTZVSYSA-N

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Laya Siroos Rezaei et al.
Environmental technology, 33(19-21), 2273-2280 (2013-02-12)
Aerobic granules can be formed in sequencing batch airlift reactors (SBAR) and sequencing batch reactors (SBR). Comparing these two systems, the SBAR has excellent mixing condition, but due to a high height-to-diameter ratio (H/D), there is no performance capability at
B V Subba Reddy et al.
The Journal of organic chemistry, 77(24), 11355-11361 (2012-12-05)
A domino cycloisomerization/Pictet-Spengler reaction of 2-(4-aminobut-1-yn-1-yl)aniline with aldehydes has been achieved using a AuIPrCl (5 mol %)/AgSbF(6) (10 mol %) catalytic system to produce the corresponding 1-aryl-N-tosyl-2,3,4,5-tetrahydropyrido[4,3-b] indole derivatives in good yields. This is the first report on the synthesis
Rongjun He et al.
Chemical communications (Cambridge, England), 49(20), 2064-2066 (2013-02-06)
Mycobacterium protein tyrosine phosphatase B (mPTPB) is essential for the survival and persistence of Mycobacterium in the host. Thus small molecule inhibitors of mPTPB are potential anti-TB agents. We developed an efficient organocatalytic multicomponent reaction (MCR) between pyrrole, formaldehyde and
Yu Qian et al.
Chemical communications (Cambridge, England), 49(26), 2700-2702 (2013-02-26)
An enantioselective four-component reaction of a diazoketone, water, an aniline and ethyl glyoxylate in the presence of catalytic Rh2(OAc)4 and a chiral Brønsted acid was developed to efficiently produce β-hydroxy-α-amino acid derivatives in good yields with high diastereoselectivity and enantioselectivity.
Ping-Xin Zhou et al.
Chemical communications (Cambridge, England), 49(6), 561-563 (2012-12-05)
Two different cyclic amino esters are synthesized by palladium-catalyzed cross-coupling reaction of diazoesters with N-substituted-2-iodoanilines. Aryldiazoacetates lead to cyclic α-amino esters with an α-quaternary carbon centre in the presence of CO. Additionally, arylvinyldiazoacetates afford cyclic α,β-unsaturated γ-amino esters.
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