Finite Group Databasebeta

C3⋊(C3⋊(C3⋊#157)) #11758156

order972
isoclinismisoclinic class of C3⋊(C3⋊(C3⋊#157))
automorphism?
homologyAbelianization (H1) = C4 · Schur multiplier (H2) = C34

Aliases

unambiguous semidirect productC3⋊(C3⋊(C3⋊#157))

Splittings

Fitting, socle, derived, SylowC35 ⋊ C4

Subgroups

subgroupG/H
center, Frattini, hypercenterC1G
commutator, Fitting, socle, hypocenterC35C4
prime radical, cosocleC33×C3⋊D3C2
LCSG ▷ C35
UCSC1

904 conjugacy classes of subgroups.

Full subgroup data →

Presentation

transitive degreeμt(G) = 108

Polycyclic presentation:

2^2,3^5|a^2=b,c^a=d,d^a=c^2,e^a=e^2,f^a=f^2,g^a=g^2,c^b=c^2,d^b=d^2

Conjugacy classes & character table

84 conjugacy classes — view the full character table.

Relationships

maximal subgroup ofD3×C3⋊(C3⋊#157), C3⋊D3×C3⋊#157, #157×C3⋊(C3⋊D3), …
maximal normal subgroup ofD3×C3⋊(C3⋊#157), C3⋊D3×C3⋊#157, #157×C3⋊(C3⋊D3), …
maximal quotient ofC3⋊(C3⋊(C3⋊#622)), C2×C3⋊(C3⋊(C3⋊#157))

GAP

Construct this group in GAP via the SmallGroups library:

gap> SmallGroup(972, 881);